Chimeric ospa genes, proteins and methods of use thereof

ABSTRACT

The invention relates to the development of chimeric OspA molecules for use in a new Lyme vaccine. More specifically, the chimeric OspA molecules comprise the proximal portion from one OspA serotype, together with the distal portion from another OspA serotype, while retaining antigenic properties of both of the parent polypeptides. The chimeric OspA molecules are delivered alone or in combination to provide protection against a variety of  Borrelia  genospecies. The invention also provides methods for administering the chimeric OspA molecules to a subject in the prevention and treatment of Lyme disease or borreliosis.

RELATED APPLICATIONS

This application is a Divisional of U.S. application Ser. No.13/107,796, filed May 13, 2011 (now U.S. Pat. No. 8,623,376, issued Jan.7, 2014), which claims benefit of U.S. Provisional Patent ApplicationSer. No. 61/334,901, filed May 14, 2010, each of which is incorporatedherein by reference in its entirety.

FIELD OF THE INVENTION

The invention generally relates to chimeric OspA polypeptides, nucleicacids encoding the polypeptides, compositions comprising thesemolecules, and methods of use thereof.

BACKGROUND OF THE INVENTION

Lyme disease is a tick-borne disease caused by Borrelia burgdorferisensu lato (s.l.). The disease is typically characterized by thedevelopment of an expanding red rash at the site of the tick bite thatmay be followed by systemic complications including meningitis, carditisor arthritis. Almost all cases of Lyme disease are caused by one ofthree genospecies, Borrelia afzelii, Borrelia garinii and Borreliaburgdorferi sensu stricto (s.s.). In Europe, all three species whichinfect humans are found. However, in North America only a singlespecies, Borrelia burgdorferi sensu stricto, is found. Borreliaburgdorferi is a species of Gram negative bacteria of the spirocheteclass of the genus Borrelia. Antibiotic treatment of Lyme disease isusually effective but some patients develop a chronic disabling form ofthe disease involving joints or nervous system, which does notsubstantially improve even after parenteral antibiotic therapy, thushighlighting the need for a vaccine for high-risk populations.

Outer surface protein A (OspA) is a 31 kDa antigen, expressed byBorrelia burgdorferi s.l. species present in the midgut of Ixodes ticks.OspA has proven to be efficacious in preventing Lyme disease in NorthAmerica (Steere et al., N. Engl. J. Med. 339: 209-15, 1998; Sigal etal., N. Engl. J. Med. 339:216-22, 1998; erratum in: N. Engl. J. Med.339:571, 1998). The amino terminus of fully processed OspA is a cysteineresidue that is post-translationally modified with three fatty-acylchains that anchor the protein to the outer surface of the bacterialmembrane (Bouchon et al., Anal. Biochem. 246: 52-61, 1997). Lipidationof OspA is reported to stabilize the molecule (Luft, personalcommunication) and is essential for protection in the absence of astrong adjuvant (Erdile et al., Infect. Immun. 61: 81-90, 1993). Asoluble, recombinant form of the protein lacking the amino-terminallipid membrane anchor was co-crystallized with the Fab fragment of anagglutinating mouse monoclonal antibody to determine the structure ofOspA, which was shown to comprise 21 anti-parallel p-strands followed bya single α-helix (Li et al., Proc. Natl. Acad. Sci. U.S.A. 94:3584-9,1997).

A monovalent OspA-based vaccine (LYMErix®) was marketed in the USA forthe prevention of Lyme disease. However, in Europe heterogeneity in OspAsequences across the three genospecies precludes broad protection with avaccine based on OspA from a single strain (Gern et al., Vaccine15:1551-7, 1997). Seven principal OspA serotypes have been recognizedamong European isolates (designated serotypes 1 to 7, Wilske et al., J.Clin. Microbiol. 31:340-50, 1993). OspA serotypes correlate withspecies; serotype 1 corresponds to B. burgdorferi s.s., serotype 2corresponds to B. afzelii and serotypes 3 to 7 correspond to B. garinii.

Protective immunity acquired through immunization with OspA is unusualsince the interaction between the host's immune response and thepathogen does not take place in the host, but in the mid-gut of the tickvector. In the case of Lyme disease, a tick acts as a vector or carrierfor the transmission of Lyme disease from animals to humans. OspAspecific antibody acquired during feeding by an infected tick preventstransmission of B. burgdorferi s.l. to the immunized mammalian host (deSilva et al., J. Exp. Med. 183: 271-5, 1996). Protection isantibody-mediated and is mainly affected through bactericidal antibodyalthough an antibody that blocks attachment of the spirochete to areceptor on the lining of the tick gut epithelium may also beefficacious (Pal et al., J. Immunol. 166: 7398-403, 2001).

Rational development of effective OspA vaccines requires identificationof the protective epitopes such as that defined by the protectivemonoclonal antibody LA-2 (Golde et al., Infect. Immun. 65: 882-9, 1997).X-ray crystallography and NMR analysis have been used to identifyimmunologically important hypervariable domains in OspA and have mappedthe LA-2 epitope to amino acids 203-257 (Ding et al., J. Mol. Biol. 302:1153-64, 2000; Luft et al. J Infect Dis. 185 (Suppl. 1): S46-51, 2002).

There is a need in the art for the development of an OspA vaccine thatcan provide broad protection against a variety of species of Borreliathat are present in the United States, Europe, and elsewhere. Thefollowing disclosure describes the specifics of such a vaccine.

SUMMARY OF THE INVENTION

The invention addresses one or more needs in the art relating to theprevention and treatment of Lyme disease or Lyme borreliosis.

The invention includes an isolated nucleic acid molecule comprising anucleotide sequence selected from the group consisting of the sequenceset forth in SEQ ID NOS: 1, 3, and 5. In some aspects, the inventionincludes an isolated nucleic acid molecule consisting of a nucleotidesequence selected from the group consisting of the sequence set forth inSEQ ID NOS: 1, 3, and 5. In other aspects, the invention includes anisolated nucleic acid molecule comprising a nucleotide sequence selectedfrom the group consisting of: (a) a nucleotide sequence with at least90, 91, 92, 93, 94, 95, 96, 97, 98, or 99 percent sequence identity witha nucleic acid molecule comprising the nucleotide sequence set forth inSEQ ID NO: 1, SEQ ID NO: 3, or SEQ ID NO: 5; and (b) a nucleotidesequence complementary to (a). In further aspects, the inventionincludes an isolated nucleic acid molecule comprising a nucleotidesequence selected from the group consisting of: (a) a nucleotidesequence encoding a polypeptide with at least 90, 91, 92, 93, 94, 95,96, 97, 98, or 99 percent sequence identity with a polypeptidecomprising an amino acid sequence set forth in SEQ ID NO: 2, SEQ ID NO:4, or SEQ ID NO: 6; and (b) a nucleotide sequence complementary to (a).In even further aspects, the invention includes an isolated nucleic acidmolecule comprising a nucleotide sequence selected from the groupconsisting of: (a) a nucleotide sequence encoding a polypeptidecomprising an amino acid sequence set forth in SEQ ID NO: 2, SEQ ID NO:4, or SEQ ID NO: 6, the polypeptide having a substitution of one to 25conservative amino acids; (b) a nucleotide sequence encoding apolypeptide comprising an amino acid sequence set forth in SEQ ID NO: 2,SEQ ID NO: 4, or SEQ ID NO: 6, the polypeptide having an insertion ofone to 25 conservative amino acids; (c) a nucleotide sequence encoding apolypeptide comprising an amino acid sequence set forth in SEQ ID NO: 2,SEQ ID NO: 4, or SEQ ID NO: 6, the polypeptide having an internaldeletion of one to 25 conservative amino acids; (d) a nucleotidesequence encoding a polypeptide comprising an amino acid sequence setforth in SEQ ID NO: 2, SEQ ID NO: 4, or SEQ ID NO: 6, the polypeptidehaving a C- and/or N-terminal truncation of one to 25 amino acids; (e) anucleotide sequence encoding a polypeptide comprising an amino acidsequence set forth in SEQ ID NO: 2, SEQ ID NO: 4, or SEQ ID NO: 6, thepolypeptide having a modification of one to 25 amino acids selected fromamino acid substitutions, amino acid insertions, amino acid deletions, aC-terminal truncation, or an N-terminal truncation; and (f) a nucleotidesequence complementary to any of (a)-(e).

The invention includes an isolated nucleic acid molecule comprising anucleotide sequence selected from the group consisting of the sequenceset forth in SEQ ID NOS: 7, 9, and 11. In some aspects, the inventionincludes an isolated nucleic acid molecule consisting of a nucleotidesequence selected from the group consisting of the sequence set forth inSEQ ID NOS: 7, 9, and 11. In additional aspects, the invention includesan isolated nucleic acid molecule comprising a nucleotide sequenceselected from the group consisting of: (a) a nucleotide sequence with atleast 90, 91, 92, 93, 94, 95, 96, 97, 98, or 99 percent sequenceidentity with a nucleic acid molecule comprising the nucleotide sequenceset forth in SEQ ID NO: 7, SEQ ID NO: 9, or SEQ ID NO: 11; and (b) anucleotide sequence complementary to (a). In further aspects, theinvention includes an isolated nucleic acid molecule comprising anucleotide sequence selected from the group consisting of: (a) anucleotide sequence encoding a polypeptide with at least 90, 91, 92, 93,94, 95, 96, 97, 98, or 99 percent sequence identity with a polypeptidecomprising an amino acid sequence set forth in SEQ ID NO: 8, SEQ ID NO:10, or SEQ ID NO: 12; and (b) a nucleotide sequence complementary to(a). In even further aspects, the invention includes an isolated nucleicacid molecule comprising a nucleotide sequence selected from the groupconsisting of: (a) a nucleotide sequence encoding a polypeptidecomprising an amino acid sequence set forth in SEQ ID NO: 8, SEQ ID NO:10, or SEQ ID NO: 12, the polypeptide having a substitution of one to 25conservative amino acids; (b) a nucleotide sequence encoding apolypeptide comprising an amino acid sequence set forth in SEQ ID NO: 8,SEQ ID NO: 10, or SEQ ID NO: 12, the polypeptide having an insertion ofone to 25 conservative amino acids; (c) a nucleotide sequence encoding apolypeptide comprising an amino acid sequence set forth in SEQ ID NO: 8,SEQ ID NO: 10, or SEQ ID NO: 12, the polypeptide having an internaldeletion of one to 25 conservative amino acids; (d) a nucleotidesequence encoding a polypeptide comprising an amino acid sequence setforth in SEQ ID NO: 8, SEQ ID NO: 10, or SEQ ID NO: 12, the polypeptidehaving a C- and/or N-terminal truncation of one to 25 amino acids; (e) anucleotide sequence encoding a polypeptide comprising an amino acidsequence set forth in SEQ ID NO: 8, SEQ ID NO: 10, or SEQ ID NO: 12, thepolypeptide having a modification of one to 25 amino acids selected fromamino acid substitutions, amino acid insertions, amino acid deletions, aC-terminal truncation, or an N-terminal truncation; and (f) a nucleotidesequence complementary to any of (a)-(e).

The invention includes vectors, host cells, and processes of producingpolypeptides by culturing the host cells discussed herein. In someaspects, the invention includes a vector comprising any of the nucleicacid molecules described herein. In other aspects, the inventionincludes a host cell that comprises such vectors. In some aspects, thehost cell is a eukaryotic cell. In other aspects, the host cell is aprokaryotic cell. In various aspects, the process of producing apolypeptide comprises culturing the host cells described herein underconditions suitable to express the polypeptide, and optionally isolatingthe polypeptide from the culture. In various aspects, the inventionincludes compositions comprising any of these chimeric nucleic acidmolecules or any vectors comprising such nucleic acid molecules and apharmaceutically acceptable carrier or carriers.

The invention includes compositions comprising any of the nucleic acidmolecules discussed herein, or any of the vectors discussed herein, anda pharmaceutically acceptable carrier. In some aspects, the inventionincludes compositions comprising at least two of the nucleic acidmolecules discussed herein and a pharmaceutically acceptable carrier,wherein the nucleic acid molecules have different nucleotide sequences.In specific aspects, the invention includes compositions comprising acombination of the nucleotide sequences set forth in SEQ ID NOS: 1, 3,and 5.

The invention includes an isolated polypeptide comprising an amino acidsequence selected from the group consisting of the sequence set forth inSEQ ID NOS: 2, 4, and 6. In some aspects, the invention includes anisolated polypeptide consisting of an amino acid sequence selected fromthe group consisting of the sequence set forth in SEQ ID NOS: 2, 4, and6. In additional aspects, the invention includes an isolated polypeptidecomprising an amino acid sequence having at least 200 amino acidresidues with at least 90, 91, 92, 93, 94, 95, 96, 97, 98, or 99 percentsequence identity to a polypeptide comprising an amino acid sequence setforth in SEQ ID NO:2, SEQ ID NO:4, or SEQ ID NO: 6. In further aspects,the invention includes an isolated polypeptide comprising an amino acidsequence selected from the group consisting of the sequence set forth inSEQ ID NOS: 8, 10, and 12. In even further aspects, the inventionincludes an isolated polypeptide consisting of an amino acid sequenceselected from the group consisting of the sequence set forth in SEQ IDNOS: 8, 10, and 12. In some aspects, the invention includes an isolatedpolypeptide comprising an amino acid sequence having at least 200 aminoacid residues with at least 90, 91, 92, 93, 94, 95, 96, 97, 98, or 99percent sequence identity to a polypeptide comprising an amino acidsequence set forth in SEQ ID NO: 8, SEQ ID NO: 10, or SEQ ID NO: 12.

The invention includes compositions comprising any of the polypeptidesdiscussed herein and a pharmaceutically acceptable carrier. In someaspects, the invention includes compositions comprising at least two ofthe polypeptides discussed herein and a pharmaceutically acceptablecarrier, wherein the polypeptides have different amino acid sequences.In specific aspects, the invention includes compositions comprising acombination of the polypeptides comprising the amino acid sequences setforth in SEQ ID NOS: 2, 4, and 6.

The invention includes immunogenic compositions. In some aspects, animmunogenic composition of the invention comprises any of thecompositions discussed herein and a pharmaceutically acceptable carrier.In various aspects, the immunogenic composition has the property ofinducing production of an antibody that specifically binds an outersurface protein A (OspA) protein. In certain aspects, the immunogeniccomposition has the property of inducing production of an antibody thatspecifically binds Borrelia. In particular aspects, the immunogeniccomposition has the property of inducing production of an antibody thatneutralizes Borrelia. In certain aspects, the Borrelia is Borreliaburgdorferi sensu lato. In particular aspects, the Borrelia is Borreliaafzelii, Borrelia garinii or Borrelia burgdorferi sensu stricto. Infurther aspects, the Borrelia is Borrelia japonica, Borrelia andersonii,Borrelia bissettii, Borrelia sinica, Borrelia turdi, Borrelia tanukii,Borrelia valaisiana, Borrelia lusitaniae, Borrelia spielmanii, Borreliamiyamotoi or Borrelia lonestar. In some aspects, the antibody isproduced by an animal. In further aspects, the animal is a mammal. Ineven further aspects, the mammal is human.

The invention includes vaccine compositions. In some aspects, a vaccinecomposition of the invention comprises any immunogenic compositiondiscussed herein and a pharmaceutically acceptable carrier. In variousaspects, the invention includes a combination vaccine. In certainaspects, a combination vaccine of the invention comprises any vaccinecomposition discussed herein in combination with at least a secondvaccine composition. In some aspects, the second vaccine compositionprotects against a tick-borne disease. In various aspects, thetick-borne disease is Rocky Mountain Spotted Fever, Babesiosis,Relapsing Fever, Colorado tick fever, Human monocytic ehrlichiosis(HME), Human granulocytic ehrlichiosis (HGE), Southern Tick-AssociatedRash Illness (STARI), Tularemia, Tick paralysis, Powassan encephalitis,Q fever, Crimean-Congo hemorrhagic fever, Cytauxzoonosis, boutonneusefever, or tick-borne encephalitis. In other aspects, the second vaccinecomposition is a vaccine selected from the group consisting of: atick-borne encephalitis vaccine, a Japanese encephalitis vaccine, and aRocky Mountain Spotted Fever vaccine. In various aspects, the secondvaccine composition has a seasonal immunization schedule compatible withimmunization against Borrelia infection or Lyme disease.

The invention includes methods for inducing an immunological response ina subject. In various aspects, such methods comprise the step ofadministering any of the immunogenic compositions or vaccinecompositions discussed herein to the subject in an amount effective toinduce an immunological response. In certain aspects, the immunologicalresponse comprises production of an anti-OspA antibody. The inventionincludes antibodies or fragments thereof that specifically bind to anyof the polypeptides described herein.

The invention includes methods for preventing or treating a Borreliainfection or Lyme disease in a subject. In various aspects, such methodscomprise the step of administering any of the vaccine compositionsdiscussed herein or any of the combination vaccines discussed herein tothe subject in an amount effective to prevent or treat the Borreliainfection or Lyme disease. In other aspects, such methods comprise thestep of administering any of the antibodies discussed herein to thesubject in an amount effective to prevent or treat the Borreliainfection or Lyme disease. In certain aspects, such methods comprise thestep of administering an antibody or fragment thereof produced byimmunizing a mammal with the vaccine composition of any one of claims28-34 to the subject in an amount effective to prevent or treat theBorrelia infection or Lyme disease. In some aspects, the antibody orfragment thereof is a hyperimmune serum, a hyperimmune plasma, or apurified immunoglobulin fraction thereof.

The invention includes methods for passively preventing a Borreliainfection or Lyme disease in a subject, the methods comprising the stepof administering an anti-OspA antibody or fragment thereof produced byimmunizing a mammal with any of the vaccine compositions discussedherein to the subject in an amount effective to prevent the Borreliainfection or Lyme disease, wherein the antibody or fragment thereof is apurified immunoglobulin preparation or an immunoglobulin fragmentpreparation.

The invention includes methods for preventing a Borrelia infection orLyme disease in a subject, the methods comprising the step ofadministering to the subject an anti-OspA monoclonal antibody orfragment thereof generated after immunizing a subject with any of thevaccine compositions discussed herein in an amount effective to preventthe Borrelia infection or Lyme disease. In some aspects, the monoclonalantibody or fragment thereof is humanized. In a particular aspect, themonoclonal antibody is F237/BK2.

The invention includes uses of compositions of the invention for thepreparation of medicaments. Other related aspects are also provided inthe instant invention.

The foregoing summary is not intended to define every aspect of theinvention, and additional aspects are described in other sections, suchas the following detailed description. The entire document is intendedto be related as a unified disclosure, and it should be understood thatall combinations of features described herein are contemplated, even ifthe combination of features are not found together in the same sentence,or paragraph, or section of this document. Other features and advantagesof the invention will become apparent from the following detaileddescription. It should be understood, however, that the detaileddescription and the specific examples, while indicating specificembodiments of the invention, are given by way of illustration only,because various changes and modifications within the spirit and scope ofthe invention will become apparent to those skilled in the art from thisdetailed description.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic overview for preparation of lipidated OspA chimeraconstructs.

FIG. 2 is the amino acid sequence of lipB sOspA 1/2²⁵¹ (SEQ ID NO: 2).

FIGS. 3A-3B show nucleotide (SEQ ID NO: 1) and deduced amino acidsequences (SEQ ID NO: 2) of lipB sOspA 1/2²⁵¹.

FIG. 4 is the amino acid sequence of lipB sOspA 6/4 (SEQ ID NO: 4).

FIGS. 5A-5B show nucleotide (SEQ ID NO: 3) and deduced amino acidsequences (SEQ ID NO: 4) of lipB sOspA 6/4.

FIG. 6 is the amino acid sequence of lipB sOspA 5/3 (SEQ ID NO: 6).

FIGS. 7A-7B show nucleotide (SEQ ID NO: 5) and deduced amino acidsequences (SEQ ID NO: 6) of lipB sOspA 5/3.

FIG. 8 depicts optimization of codon usage for high level expression.

FIG. 9 shows sequence differences between lipidated and non-lipidatedconstructs.

FIG. 10 is a description of the T7 expression system.

FIG. 11 is an SDS-PAGE showing expression of the novel recombinant OspAproteins from induced and un-induced cultures.

FIG. 12 is a map of plasmid pUC18.

FIG. 13 is a map of plasmid pET30a.

FIG. 14 shows the strategy for creation of the lipB sOspA 5/3 Kpn I-BamHI fragment.

FIG. 15 is an alignment highlighting the amino acid change (SEQ ID NO:39) in lipB sOspA 1/2²⁵¹ and the PCR primer sequences (SEQ ID NOS: 21and 41) used to introduce the change (lipB OspA 1/2 mod (SEQ ID NO: 38);consensus sequence (SEQ ID NO: 40)).

FIGS. 16A-16B are an alignment of OspA sequence of Blip OspA BPBP/A1with the modified molecule lipB sOspA 1/2²⁵¹. The top strand is theoriginal sequence (SEQ ID NO: 42) and the bottom strand is the optimizedsequence (SEQ ID NO: 43). Note: Three bases (CAT) at the start of thesequence are not shown; they form part of the Nde I site CATATG.

FIGS. 17A-17B are an alignment of OspA sequence of Blip OspA KT with themodified molecule lipB sOspA 6/4. The top strand is the originalsequence (SEQ ID NO: 44) and the bottom strand is the optimized sequence(SEQ ID NO: 45). Note: A single base (C) at the start of the sequence isnot shown; they form part of the Nde I site CATATG.

FIGS. 18A-18B are an alignment of OspA sequence of Blip OspA 5/3 withthe modified molecule lipB sOspA 5/3. The top strand is the originalsequence (SEQ ID NO: 46) and the bottom strand is the optimized sequence(SEQ ID NO: 47).

FIG. 19 shows the distribution of functional anti-OspA responses inantibody surface binding and growth inhibition assays among protectedand infected animals immunized with 3 ng of OspA 1/2 before challengewith B. burgdorferi s.s. B31 strain. Mann-Whitney p values demonstrateda highly significant difference in functional antibody content betweenprotected and infected animals.

FIG. 20 shows the distribution of functional anti-OspA responses inantibody surface binding and growth inhibition assays among protectedand infected animals immunized with 3 ng of OspA 1/2 before challengewith feral ticks. Mann-Whitney p values demonstrated a highlysignificant difference in functional antibody content between protectedand infected animals.

FIG. 21 shows surface binding (mean fluorescence intensities (MFI)) andgrowth inhibition (GI-50 titers) in pooled mouse sera after immunizationwith three doses of the 3-component chimeric OspA vaccine. Efficientsurface binding and growth inhibition were detected against all sixBorrelia strains expressing OspA types homologous to the OspA types inthe vaccine (types 1-6).

FIG. 22 shows mean fluorescence intensity (MFI) titers that wereobtained using day 42 sera from individual mice immunized withcombinations of rOspA vaccines in a surface binding assay (SBA). Resultsshowed that all three rOspA components (1/2, 6/4, and 5/3) are requiredin a multivalent vaccine to induce high titers of surface binding IgGantibodies against all 6 strains in C3H mice. Two-component vaccines didnot fully cover the 2 missing strains.

FIG. 23 shows the growth inhibition of Borreliae using day 42 sera fromindividual mice (in groups of 10) immunized with combinations of rOspAvaccines. Only the multivalent vaccine (the vaccine comprising all threestrains) gave >50% growth inhibition in >90% of the animals (n=10). Barsin black (solid bars) indicate the strains homologous to the vaccineused.

FIG. 24 shows the coverage of Borreliae expressing intra-type variantsof OspA. Surface binding was categorized into strong (fluorescenceincreased >10-fold) or weaker (fluorescence increased 2-10-fold).

DETAILED DESCRIPTION OF THE INVENTION

The invention provides chimeric OspA molecules that are useful asantigens that can be delivered as an immunogenic composition or vaccinecomposition for Lyme disease or a Borrelia infection. Before anyembodiments of the invention are explained in detail, it is to beunderstood that the invention is not limited in its application to thedetails of construction and the arrangement of components set forth inthe following description or illustrated in the figures and examples.The section headings used herein are for organizational purposes onlyand are not to be construed as limiting the subject matter described.All references cited in this application are expressly incorporated byreference herein.

The invention embraces other embodiments and is practiced or carried outin various ways. Also, it is to be understood that the phraseology andterminology used herein is for the purpose of description and should notbe regarded as limiting. The terms “including,” “comprising,” or“having” and variations thereof are meant to encompass the items listedthereafter and equivalents thereof as well as additional items.

Embodiments of the invention are exemplified in the design and synthesisof three chimeric OspA coding sequences that encode three distinctlipidated OspA molecules, all of which share some common features. Eachchimeric coding sequence represents two OspA serotypes and the chimericcoding sequences were designed to encode stable chimeric OspA moleculesthat are safe and highly immunogenic, and afford a subject protectionagainst infection with B. burgdorferi sensu lato (s.l.).

In one aspect, the chimeric OspA molecules comprise the proximal portionfrom one OspA serotype, together with the distal portion from anotherOspA serotype while retaining the protective properties of both of theparent polypeptides. The chimeric OspA nucleic acid molecules wereexpressed in Escherichia coli (E. coli) to provide antigens which couldbe formulated as a combination vaccine to provide protection against allsix prevalent serotypes (serotypes 1-6) associated with Lyme disease orBorrelia infection in Europe and against the single OspA serotypeassociated with Lyme disease or Borrelia infection in North America.Because a vaccine comprising serotypes 1-6 provides protection againstB. afzelii, B. garinii, and B. burgdorferi, the vaccine is designed forglobal use.

The invention also includes the preparation of a second set of chimericOspA coding sequences which is, in one aspect, derived from the firstset of three genes, by removing nucleic acid sequences encoding a leadersequence needed to produce a lipidated OspA molecule. The two sets ofconstructs (giving rise to lipidated and non-lipidated polypeptides)were needed to evaluate their ease of production in the fermentor(biomass, stability, product yields etc.), to assess how readilydifferent types of antigen can be purified and to compare theirbiological characteristics (safety profile and protective potency).

The invention includes immunogenic compositions comprising the chimericOspA molecules of the invention. The invention likewise includesvaccines and vaccine kits comprising such OspA molecules, processes formaking the immunogenic compositions and vaccines and the use of theimmunogenic compositions and vaccines in human and veterinary medicaltherapy and prevention. The invention further includes methods ofimmunizing against Lyme disease or Borrelia infection using the OspAcompositions described herein and the use of the OspA compositions inthe manufacture of a medicament for the prevention of Lyme disease orBorrelia infection.

DEFINITIONS

Unless otherwise defined, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which this invention belongs. The following referencesprovide one of skill with a general definition of many of the terms usedin this invention: Singleton, et al., DICTIONARY OF MICROBIOLOGY ANDMOLECULAR BIOLOGY (2d ed. 1994); THE CAMBRIDGE DICTIONARY OF SCIENCE ANDTECHNOLOGY (Walker ed., 1988); THE GLOSSARY OF GENETICS, 5TH ED., R.Rieger, et al. (eds.), Springer Verlag (1991); and Hale and Marham, THEHARPER COLLINS DICTIONARY OF BIOLOGY (1991).

The following abbreviations are used throughout.

-   AA Amino acid-   Amp Ampicillin-   bp Base pairs-   B. afzelii Borrelia afzelii-   B. burdorferi Borrelia burgdorferi-   B. garinii Borrelia garinii-   DNA Deoxyribonucleic acid-   dNTPs Deoxynucleotide triphosphate-   E. coli Escherichia coli-   GC content Percentage of a sequence containing bases Guanine and    Cytosine-   hLFA-1 Human leukocyte function-associated antigen-1-   HPLC High Performance Liquid Chromatography-   IP Intellectual property-   IPTG Isopropyl-beta-D-thiogalactopyranoside-   Kan Kanamycin-   kDa KiloDaltons-   LB Luria Broth-   Lip B Leader sequence from Outer surface protein B-   Mab Monoclonal antibody-   OD Optical density-   OspA Outer surface protein A-   OspB Outer surface protein B-   PCR Polymerase chain reaction-   RNA Ribonucleic acid-   s.l. Sensu lato-   s.s. Sensu stricto-   SDS Sodium dodecyl sulfate-   SMK Growth media for E. coli (ketoglutarate sorbitol media)-   tRNA Transfer ribonucleic acid-   WCB Working cell bank

It is noted here that, as used in this specification and the appendedclaims, the singular forms “a,” “an,” and “the” include plural referenceunless the context clearly dictates otherwise.

As used herein, the following terms have the meanings ascribed to themunless specified otherwise.

The term “gene” refers to a DNA sequence that encodes a sequence ofamino acids which comprise all or part of one or more polypeptides,proteins or enzymes, and may or may not include introns, and regulatoryDNA sequences, such as promoter or enhancer sequences, 5′-untranslatedregion, or 3′-untranslated region which affect, for example, theconditions under which the gene is expressed. In the present disclosure,the OspA gene is bacterial and, therefore, there are no introns. Theterm “coding sequence” refers to a DNA sequence that encodes a sequenceof amino acids, but does not contain introns or regulatory sequences.Likewise, in the present disclosure the OspA coding sequence does notcontain regulatory sequences.

“Nucleic acid” or “nucleic acid sequence” or “nucleic acid molecule”refers to deoxyribonucleotides or ribonucleotides and polymers thereofin either single- or double-stranded form. The term encompasses nucleicacids containing known nucleotide analogs or modified backbone residuesor linkages, which are synthetic, naturally occurring, and non-naturallyoccurring, which have similar binding properties as the referencenucleic acid, and which are metabolized in a manner similar to thereference nucleotides. Examples of such analogs include, withoutlimitation, phosphorothioates, phosphoramidates, methyl phosphonates,chiral-methyl phosphonates, 2-O-methyl ribonucleotides, peptide-nucleicacids (PNAs). The terms encompass molecules formed from any of the knownbase analogs of DNA and RNA such as, but not limited to4-acetylcytosine, 8-hydroxy-N6-methyladenine, aziridinyl-cytosine,pseudoisocytosine, 5-(carboxyhydroxylmethyl) uracil, 5-fluorouracil,5-bromouracil, 5-carboxymethylaminomethyl-2-thiouracil,5-carboxy-methylaminomethyluracil, dihydrouracil, inosine,N6-iso-pentenyladenine, 1-methyladenine, 1-methylpseudouracil,1-methylguanine, 1-methylinosine, 2,2-dimethyl-guanine, 2-methyladenine,2-methylguanine, 3-methylcytosine, 5-methylcytosine, N6-methyladenine,7-methylguanine, 5-methylaminomethyluracil,5-methoxyamino-methyl-2-thiouracil, beta-D-mannosylqueosine,5′-methoxycarbonyl-methyluracil, 5-methoxyuracil,2-methylthio-N6-isopentenyladenine, uracil-5-oxyacetic acid methylester,uracil-5-oxyacetic acid, oxybutoxosine, pseudouracil, queosine,2-thiocytosine, 5-methyl-2-thiouracil, 2-thiouracil, 4-thiouracil,5-methyluracil, N-uracil-5-oxyacetic acid methylester,uracil-5-oxyacetic acid, pseudouracil, queosine, 2-thiocytosine, and2,6-diaminopurine.

Unless otherwise indicated, a particular nucleic acid sequence alsoimplicitly encompasses conservatively modified variants thereof (e.g.,degenerate codon substitutions) and complementary sequences, as well asthe sequence explicitly indicated. Specifically, degenerate codonsubstitutions, in some aspects, are achieved by generating sequences inwhich the third position of one or more selected (or all) codons issubstituted with mixed-base and/or deoxyinosine residues (Batzer et al.,Nucleic Acid Res. 19:5081 (1991); Ohtsuka et al., J. Biol. Chem.260:2605-2608 (1985); Rossolini et al., Mol. Cell. Probes 8:91-98(1994)). The term nucleic acid is used interchangeably with gene, cDNA,mRNA, oligonucleotide, and polynucleotide.

The terms “polypeptide,” “peptide” and “protein” are usedinterchangeably herein to refer to a polymer of amino acid residueslinked via peptide bonds. The terms apply to amino acid polymers inwhich one or more amino acid residue is an artificial chemical mimeticof a corresponding naturally occurring amino acid, as well as tonaturally occurring amino acid polymers and non-naturally occurringamino acid polymers. The term “protein” typically refers to largepolypeptides. The term “peptide” typically refers to short polypeptides.Synthetic polypeptides can be synthesized, for example, using anautomated polypeptide synthesizer.

The term “Osp A molecule” or “chimeric OspA molecule” refers, in oneaspect, to an “OspA nucleic acid” comprising the nucleotide sequence ofSEQ ID NO: 1 (lipB sOspA 1/2²⁵¹), SEQ ID NO: 3 (lipB sOspA 6/4), SEQ IDNO: 5 (lipB sOspA 5/3), SEQ ID NO: 7 (sOspA 1/2²⁵¹), SEQ ID NO: 9 (sOspA6/4), SEQ ID NO: 11 (sOspA 5/3), SEQ ID NO: 168 (orig sOspA 1/2), SEQ IDNO: 170 (orig sOspA 6/4), or SEQ ID NO: 172 (orig sOspA 5/3), or, inanother aspect to an “OspA polypeptide” comprising the amino acidsequence of SEQ ID NO: 2 (lipB sOspA 1/2²⁵¹), SEQ ID NO: 4 (lipB sOspA6/4), SEQ ID NO: 6 (lipB sOspA 5/3), SEQ ID NO: 8 (sOspA 1/2²⁵¹), SEQ IDNO: 10 (sOspA 6/4), SEQ ID NO: 12 (sOspA 5/3), SEQ ID NO: 169 (origsOspA 1/2), SEQ ID NO: 171 (orig sOspA 6/4), or SEQ ID NO: 173 (origsOspA 5/3).

The term “lipB sOspA molecule” refers, in one aspect, to an “OspAnucleic acid” comprising the nucleotide sequence of SEQ ID NO: 1 (lipBsOspA 1/2²⁵¹), SEQ ID NO: 3 (lipB sOspA 6/4), or SEQ ID NO: 5 (lipBsOspA 5/3) or, in another aspect to an “OspA polypeptide” comprising theamino acid sequence of SEQ ID NO: 2 (lipB sOspA 1/2²⁵¹), SEQ ID NO: 4(lipB sOspA 6/4), or SEQ ID NO: 6 (lipB sOspA 5/3). The nucleic acidsequences of SEQ ID NOS: 7, 9, and 11 lack the nucleic acid sequenceencoding the lipB leader sequence (MRLLIGFALALALIG (SEQ ID NO: 13). Inaddition, the nucleic acid sequences of SEQ ID NOS: 7, 9, and 11 encodea methionine residue at the amino terminus of SEQ ID NOS: 8, 10, and 12in place of the cysteine residue present at the carboxy terminus of thelipB leader sequence in SEQ ID NOS: 2, 4, and 6.

The term “orig sOspA molecule” or “original sOspA molecule” refers, inone aspect, to an “OspA nucleic acid” comprising the nucleotide sequenceof SEQ ID NO: 168 (orig sOspA 1/2), SEQ ID NO: 170 (orig sOspA 6/4), orSEQ ID NO: 172 (orig sOspA 5/3) or, in another aspect to an “OspApolypeptide” comprising the amino acid sequence of SEQ ID NO: 169 (origsOspA 1/2), SEQ ID NO: 171 (orig sOspA 6/4), or SEQ ID NO: 173 (origsOspA 5/3). These “original” molecules are chimeric constructs withoutmutations and without codon optimization.

The invention includes “lipidated OspA” and “non-lipidated OspA”chimeric molecules. In various aspects, lipidation confers adjuvantproperties on OspA. In some aspects of the invention, the lipidated OspAmolecules comprise an OspB leader sequence. In some aspects of theinvention, the OspB leader sequence comprises amino acidsMRLLIGFALALALIG (SEQ ID NO: 13). In other aspects, the OspB leadersequence comprises other amino acids.

The terms “identical” or percent “identity” as known in the art refersto a relationship between the sequences of two or more polypeptidemolecules or two or more nucleic acid molecules, as determined bycomparing the sequences. In the art, “identity” also means the degree ofsequence relatedness between nucleic acid molecules or polypeptides, asthe case may be, as determined by the match between strings of two ormore nucleotide or two or more amino acid sequences. “Identity” measuresthe percent of identical matches between the smaller of two or moresequences with gap alignments (if any) addressed by a particularmathematical model or computer program (i.e., “algorithms”).“Substantial identity” refers to sequences with at least about 70%,about 71%, about 72%, about 73%, about 74%, about 75%, about 76%, about77%, about 78%, about 79%, about 80%, about 81%, about 82%, about 83%,about 84%, about 85%, about 86%, about 87%, about 88%, about 89%, about90%, about 91%, about 92%, about 93%, about 94%, about 95%, about 96%,about 97%, about 98%, or about 99% sequence identity over a specifiedsequence. In some aspects, the identity exists over a region that is atleast about 50-100 amino acids or nucleotides in length. In otheraspects, the identity exists over a region that is at least about100-200 amino acids or nucleotides in length. In other aspects, theidentity exists over a region that is at least about 200-500 amino acidsor nucleotides in length. In certain aspects, percent sequence identityis determined using a computer program selected from the groupconsisting of GAP, BLASTP, BLASTN, FASTA, BLASTA, BLASTX, BestFit andthe Smith-Waterman algorithm

It also is specifically understood that any numerical value recitedherein includes all values from the lower value to the upper value,i.e., all possible combinations of numerical values between the lowestvalue and the highest value enumerated are to be considered to beexpressly stated in this application. For example, if a concentrationrange is stated as about 1% to 50%, it is intended that values such as2% to 40%, 10% to 30%, or 1% to 3%, etc., are expressly enumerated inthis specification. The values listed above are only examples of what isspecifically intended.

Ranges, in various aspects, are expressed herein as from “about” or“approximately” one particular value and/or to “about” or“approximately” another particular value. When values are expressed asapproximations, by use of the antecedent “about,” it will be understoodthat some amount of variation is included in the range.

The term “similarity” is a related concept but, in contrast to“identity”, refers to a measure of similarity which includes bothidentical matches and conservative substitution matches. If twopolypeptide sequences have, for example, 10/20 identical amino acids,and the remainder are all non-conservative substitutions, then thepercent identity and similarity would both be 50%. If, in the sameexample, there are five more positions where there are conservativesubstitutions, then the percent identity remains 50%, but the percentsimilarity would be 75% (15/20). Therefore, in cases where there areconservative substitutions, the degree of percent similarity between twopolypeptides will be higher than the percent identity between those twopolypeptides.

The term “isolated nucleic acid molecule” refers to a nucleic acidmolecule of the invention that (1) has been separated to any degree fromproteins, lipids, carbohydrates or other materials with which it isnaturally found when total DNA is isolated from the source cells, (2) isnot linked to all or a portion of a polynucleotide to which the“isolated nucleic acid molecule” is linked in nature, (3) is operablylinked to a polynucleotide which it is not linked to in nature, or (4)does not occur in nature as part of a larger polynucleotide sequence.Substantially free as used herein indicates that the nucleic acidmolecule is free from any other contaminating nucleic acid molecule(s)or other contaminants that are found in its natural environment thatwould interfere with its use in polypeptide production or itstherapeutic, diagnostic, prophylactic or research use.

The term “isolated polypeptide” refers to a polypeptide of the presentinvention that (1) has been separated to any degree frompolynucleotides, lipids, carbohydrates or other materials with which itis naturally found when isolated from the source cell, (2) is not linked(by covalent or noncovalent interaction) to all or a portion of apolypeptide to which the “isolated polypeptide” is linked in nature, (3)is operably linked (by covalent or noncovalent interaction) to apolypeptide with which it is not linked in nature, or (4) does not occurin nature. In one aspect, the isolated polypeptide is substantially freefrom any other contaminating polypeptides or other contaminants that arefound in its natural environment that would interfere with itstherapeutic, diagnostic, prophylactic or research use.

As used herein a “fragment” of a polypeptide refers to any portion ofthe polypeptide smaller than the full-length polypeptide or proteinexpression product. Fragments are typically deletion analogs of thefull-length polypeptide wherein one or more amino acid residues havebeen removed from the amino terminus and/or the carboxy terminus of thefull-length polypeptide. Accordingly, “fragments” are a subset ofdeletion analogs described below.

As used herein an “analog” refers to a polypeptide substantially similarin structure and having the same biological activity, albeit in certaininstances to a differing degree, to a naturally-occurring molecule.Analogs differ in the composition of their amino acid sequences comparedto the naturally-occurring polypeptide from which the analog is derived,based on one or more mutations involving (i) deletion of one or moreamino acid residues at one or more termini of the polypeptide (includingfragments as described above) and/or one or more internal regions of thenaturally-occurring polypeptide sequence, (ii) insertion or addition ofone or more amino acids at one or more termini (typically an “addition”analog) of the polypeptide and/or one or more internal regions(typically an “insertion” analog) of the naturally-occurring polypeptidesequence or (iii) substitution of one or more amino acids for otheramino acids in the naturally-occurring polypeptide sequence.Substitutions are conservative or non-conservative based on thephysico-chemical or functional relatedness of the amino acid that isbeing replaced and the amino acid replacing it.

“Conservatively modified analogs” applies to both amino acid and nucleicacid sequences. With respect to particular nucleic acid sequences,conservatively modified nucleic acids refers to those nucleic acidswhich encode identical or essentially identical amino acid sequences, orwhere the nucleic acid does not encode an amino acid sequence, toessentially identical sequences. Because of the degeneracy of thegenetic code, a large number of functionally identical nucleic acidsencode any given protein. For instance, the codons GCA, GCC, GCG and GCUall encode the amino acid alanine. Thus, at every position where analanine is specified by a codon, the codon can be altered to any of thecorresponding codons described without altering the encoded polypeptide.Such nucleic acid variations are “silent variations,” which are onespecies of conservatively modified analogs. Every nucleic acid sequenceherein which encodes a polypeptide also describes every possible silentvariation of the nucleic acid. One of skill will recognize that eachcodon in a nucleic acid (except AUG, which is ordinarily the only codonfor methionine, and TGG, which is ordinarily the only codon fortryptophan) can be modified to yield a functionally identical molecule.Accordingly, each silent variation of a nucleic acid which encodes apolypeptide is implicit in each described sequence.

As to amino acid sequences, one of skill will recognize that individualsubstitutions, insertions, deletions, additions, or truncations to anucleic acid, peptide, polypeptide, or protein sequence which alters,adds or deletes a single amino acid or a small percentage of amino acidsin the encoded sequence is a “conservatively modified analog” where thealteration results in the substitution of an amino acid with achemically similar amino acid. Conservative substitution tablesproviding functionally similar amino acids are well known in the art.Such conservatively modified variants are in addition to and do notexclude polymorphic variants, interspecies homologs, and alleles of theinvention.

The following eight groups each contain amino acids that areconservative substitutions for one another:

1) Alanine (A), Glycine (G);

2) Aspartic acid (D), Glutamic acid (E);

3) Asparagine (N), Glutamine (Q); 4) Arginine (R), Lysine (K); 5)Isoleucine (I), Leucine (L), Methionine (M), Valine (V); 6)Phenylalanine (F), Tyrosine (Y), Tryptophan (W); 7) Serine (S),Threonine (T); and

8) Cysteine (C), Methionine (M) (see, e.g., Creighton, Proteins (1984)).

As used herein a “variant” refers to a polypeptide, protein or analogthereof that comprises at least one amino acid substitution, deletion,insertion, or modification, provided that the variant retains thebiological activity of the native polypeptide.

As used herein an “allelic variant” refers to any of two or morepolymorphic forms of a gene occupying the same genetic locus. Allelicvariations arise naturally through mutation and, in some aspects, resultin phenotypic polymorphism within populations. In certain aspects, genemutations are silent (no change in the encoded polypeptide) or, in otheraspects, encode polypeptides having altered amino acid sequences.“Allelic variants” also refer to cDNAs derived from mRNA transcripts ofgenetic allelic variants, as well as the proteins encoded by them.

The term “derivative” refers to polypeptides that are covalentlymodified by conjugation to therapeutic or diagnostic agents, labeling(e.g., with radionuclides or various enzymes), covalent polymerattachment such as pegylation (derivatization with polyethylene glycol)and insertion or substitution by chemical synthesis of non-natural aminoacids. In some aspects, derivatives are modified to comprise additionalchemical moieties not normally a part of the molecule. Such moieties, invarious aspects, modulate the molecule's solubility, absorption, and/orbiological half-life. The moieties, in various other aspects,alternatively decrease the toxicity of the molecule and eliminate orattenuate any undesirable side effect of the molecule, etc. Moietiescapable of mediating such effects are disclosed in Remington'sPharmaceutical Sciences (1980). Procedure for coupling such moieties toa molecule are well known in the art. For example, in some aspects, anOspA derivative is an OspA molecule having a chemical modification whichconfers a longer half-life in vivo to the protein. In one embodiment,the polypeptides are modified by addition of a water soluble polymerknown in the art. In a related embodiment, polypeptides are modified byglycosylation, PEGylation, and/or polysialylation.

The term “recombinant” when used with reference, e.g., to a cell, ornucleic acid, protein, or vector, indicates that the cell, nucleic acid,protein or vector, has been modified by the introduction of aheterologous nucleic acid or protein or the alteration of a nativenucleic acid or protein, or that the cell is derived from a cell somodified. Thus, for example, recombinant cells express genes that arenot found within the native (non-recombinant) form of the cell orexpress native genes that are otherwise abnormally expressed,underexpressed or not expressed at all.

As used herein “selectable marker” refers to a gene encoding an enzymeor other protein that confers upon the cell or organism in which it isexpressed an identifiable phenotypic change such as resistance to adrug, antibiotic or other agent, such that expression or activity of themarker is selected for (for example, but without limitation, a positivemarker, such as the neo gene) or against (for example, and withoutlimitation, a negative marker, such as the diphtheria gene). A“heterologous selectable marker” refers to a selectable marker gene thathas been inserted into the genome of an animal in which it would notnormally be found.

Examples of selectable markers include, but are not limited to, anantibiotic resistance gene such as neomycin (neo), puromycin (Puro),diphtheria toxin, phosphotransferase, hygromycin phosphotransferase,xanthineguanine phosphoribosyl transferase, the Herpes simplex virustype 1 thymidine kinase, adenine phosphoribosyltransferase andhypoxanthine phosphonbosyltransferase. The worker of ordinary skill inthe art will understand any selectable marker known in the art is usefulin the methods described herein.

The term “heterologous” when used with reference to portions of anucleic acid indicates that the nucleic acid comprises two or moresubsequences that are not found in the same relationship to each otherin nature. For instance, the nucleic acid is typically recombinantlyproduced, having two or more sequences from unrelated genes arranged tomake a new functional nucleic acid, e.g., a promoter from one source anda coding region from another source. Similarly, a heterologous proteinindicates that the protein comprises two or more subsequences that arenot found in the same relationship to each other in nature (e.g., afusion protein).

As used herein, the term “homologous” refers to the relationship betweenproteins that possess a “common evolutionary origin,” including proteinsfrom superfamilies (e.g., the immunoglobulin superfamily) and homologousproteins from different species (e.g., myosin light chain, etc.) (Reecket al., Cell 50:667, 1987). Such proteins (and their encoding genes)have sequence homology, as reflected by their sequence similarity,whether in terms of percent similarity or the presence of specificresidues or motifs at conserved positions.

Optimal alignment of sequences for comparison is conducted, for exampleand without limitation, by the local homology algorithm of Smith et al.,Adv. Appl. Math. 2:482, 1981; by the homology alignment algorithm ofNeedleman et al., J. Mol. Biol. 48:443, 1970; by the search forsimilarity method of Pearson et al., Proc. Natl. Acad. Sci. USA 85:2444,1988; by computerized implementations of these algorithms (GAP, BESTFIT,FASTA, and TFASTA in the Wisconsin Genetics Software Package, GeneticsComputer Group, 575 Science Dr., Madison, Wis.), or by visual inspection(see generally Ausubel et al., supra). Another example of algorithm thatis suitable for determining percent sequence identity and sequencesimilarity is the BLAST algorithm, which is described in Altschul etal., J. Mol. Biol. 215:403-410, 1990. Software for performing BLASTanalyses is publicly available through the National Center forBiotechnology Information. In addition to calculating percent sequenceidentity, the BLAST algorithm also performs a statistical analysis ofthe similarity between two sequences (see, e.g., Karlin et al., Proc.Natl. Acad. Sci. USA 90:5873-5787, 1993).

The term “vector” is used to refer to any molecule (e.g., nucleic acid,plasmid or virus) used to transfer coding information to a host cell.

A “cloning vector” is a small piece of DNA into which a foreign DNAfragment can be inserted. The insertion of the fragment into the cloningvector is carried out by treating the vehicle and the foreign DNA withthe same restriction enzyme, then ligating the fragments together. Thereare many types of cloning vectors and all types of cloning vectors areused in the invention. Genetically engineered plasmids andbacteriophages (such as phage A) are perhaps most commonly used for thispurpose. Other types of cloning vectors include bacterial artificialchromosomes (BACs) and yeast artificial chromosomes (YACs).

An “expression vector” is a nucleic acid construct, generatedrecombinantly or synthetically, with a series of specified nucleic acidelements that permit transcription of a particular nucleic acid in ahost cell. The expression vector can be part of a plasmid, virus, ornucleic acid fragment. In certain aspects, the expression vectorincludes a nucleic acid to be transcribed operably linked to a promoter.

The term “coding sequence” is defined herein as a nucleic acid sequencethat is transcribed into mRNA, which is translated into a polypeptidewhen placed under the control of the appropriate control sequences. Theboundaries of the coding sequence are generally determined by the ATGstart codon, which is normally the start of the open reading frame atthe 5′ end of the mRNA and a transcription terminator sequence locatedjust downstream of the open reading frame at the 3′ end of the mRNA. Acoding sequence can include, but is not limited to, genomic DNA, cDNA,semisynthetic, synthetic, and recombinant nucleic acid sequences. In oneaspect, a promoter DNA sequence is defined by being the DNA sequencelocated upstream of a coding sequence associated thereto and by beingcapable of controlling the expression of this coding sequence.

A “promoter” is defined as an array of nucleic acid control sequencesthat direct transcription of a nucleic acid. As used herein, a promoterincludes necessary nucleic acid sequences near the start site oftranscription, such as, in the case of a polymerase II type promoter, aTATA element. A promoter also optionally includes distal enhancer orrepressor elements, which can be located as much as several thousandbase pairs from the start site of transcription. A “constitutive”promoter is a promoter that is active under most environmental anddevelopmental conditions. An “inducible” promoter is a promoter that isactive under environmental or developmental regulation.

The term “operably linked” refers to a functional linkage between anucleic acid expression control sequence (such as a promoter, or arrayof transcription factor binding sites) and a second nucleic acidsequence, wherein the expression control sequence directs transcriptionof the nucleic acid corresponding to the second sequence.

The term “transduction” is used to refer to the transfer of nucleicacids from one bacterium to another, usually by a phage. “Transduction”also refers to the acquisition and transfer of eukaryotic cellularsequences by retroviruses.

The term “transfection” is used to refer to the uptake of foreign orexogenous DNA by a cell, and a cell has been “transfected” when theexogenous DNA has been introduced inside the cell membrane. A number oftransfection techniques are well known in the art and are disclosedherein. See, for example, Graham et al., Virology, 52:456 (1973);Sambrook et al., Molecular Cloning, a Laboratory Manual, Cold SpringHarbor Laboratories, New York, (1989); Davis et al., Basic Methods inMolecular Biology, Elsevier, (1986); and Chu et al., Gene, 13:197(1981). Such techniques can be used to introduce one or more exogenousDNA moieties into suitable host cells.

The term “transformation” as used herein refers to a change in a cellsgenetic characteristics, and a cell has been transformed when it hasbeen modified to contain new DNA. For example, a cell is transformedwhere it is genetically modified from its native state. Followingtransfection or transduction, the transforming DNA may recombine withthat of the cell by physically integrating into a chromosome of thecell. In some instances, the DNA is maintained transiently as anepisomal element without being replicated, or it replicatesindependently as a plasmid. A cell is considered to have been stablytransformed when the DNA is replicated with the division of the cell.

The term “endogenous” refers to a polypeptide or polynucleotide or othercompound that is expressed naturally in the host organism, or originateswithin a cell, tissue or organism. “Exogenous” refers to a polypeptide,polynucleotide or other compound that originates outside a cell, tissueor organism.

The term “agent” or “compound” describes any molecule, e.g. protein orpharmaceutical, with the capability of affecting a biological parameterin the invention.

A “control,” as used herein, can refer to an active, positive, negativeor vehicle control. As will be understood by those of skill in the art,controls are used to establish the relevance of experimental results,and provide a comparison for the condition being tested.

The term “reduces the severity,” when referring to a symptom of Lyme orLyme disease, means that the symptom has delayed onset, reducedseverity, or causes less damage to the subject. Generally, severity of asymptom is compared to a control, e.g., that does not receive an activeprophylactic or therapeutic composition. In that case, a composition canbe said to reduce the severity of a symptom of Lyme if the symptom isreduced by 10%, 25%, 30%, 50%, 80%, or 100% (i.e., essentiallyeliminated), as compared to the control level of the symptom.

The term “antigen” refers to a molecule or a portion of a moleculecapable of being bound by a selective binding agent, such as anantibody, and additionally capable of being used in a subject to produceantibodies capable of binding to an epitope of each antigen. An antigen,in various aspects, has one or more epitopes.

The term “antibody” refers to a molecule or molecules having specificityfor an OspA polypeptide. As used herein the terms, “specific,”“specificity,” and “specifically binds” refer to the ability of theantibody to bind to OspA polypeptides and not to bind to non-OspApolypeptides. In certain aspects, the antibody is a “neutralizingantibody,” wherein the antibody reacts with an infectious agent anddestroys or inhibits its infectiveness or virulence. The inventionincludes immunogenic compositions comprising antibodies that“neutralize” Borrelia.

The terms “pharmaceutically acceptable carrier” or “physiologicallyacceptable carrier” as used herein refer to one or more formulationmaterials suitable for accomplishing or enhancing the delivery of theOspA polypeptide, OspA nucleic acid molecule or OspA antibody as apharmaceutical composition.

The term “stabilizer” refers to a substance or vaccine excipient whichprotects the immunogenic composition of the vaccine from adverseconditions, such as those which occur during heating or freezing, and/orprolongs the stability or shelf-life of the immunogenic composition in astable and immunogenic condition or state. Examples of stabilizersinclude, but are not limited to, sugars, such as sucrose, lactose andmannose; sugar alcohols, such as manitol; amino acids, such as glycineor glutamic acid; and proteins, such as human serum albumin or gelatin.

The term “antimicrobial preservative” refers to any substance which isadded to the immunogenic composition or vaccine that inhibits the growthof microorganisms that may be introduced upon repeated puncture ofmultidose vials, should such containers be used. Examples ofantimicrobial preservatives include, but are not limited to, substancessuch as thimerosal, 2-phenoxyethanol, benzethonium chloride, and phenol.

The term “immunogenic composition” refers to a composition comprising anantigen (e.g., chimeric OspA molecules) against which antigen-specificantibodies are raised, an adjuvant that stimulates the subject host'simmune response, and a suitable immunologically-inert,pharmaceutically-acceptable carrier. Optionally, an immunogeniccomposition comprises one or more stabilizers. Optionally, animmunogenic composition comprises one or more antimicrobialpreservatives.

The terms “vaccine” or “vaccine composition” refer to a biologicalpreparation that improves immunity to a particular disease (e.g., Lymedisease or Borrelia infection). A vaccine typically contains an agentthat resembles a disease-causing microorganism (e.g., chimeric OspAmolecules (antigen) of Borrelia). The agent stimulates the body's immunesystem to recognize the agent as foreign, destroy it, and “remember” it,so that the immune system can more easily recognize and destroy any ofthese microorganisms that it later encounters. Vaccines, in variousaspects, are prophylactic (prevent or ameliorate the effects of a futureinfection by any natural or “wild” pathogen), or therapeutic (vaccinesagainst present infection). As set forth above, such vaccinecompositions include formulations comprising pharmaceutically acceptablecarriers. Optionally, a vaccine also comprises one or more stabilizersand/or one or more antimicrobial preservatives.

The terms “effective amount” and “therapeutically effective amount” eachrefer to the amount of nucleic acid molecule, polypeptide, composition,or antibody used to support an observable level of one or morebiological activities of the OspA polypeptides as set forth herein. Forexample, an effective amount, in some aspects of the invention, would bethe amount necessary to prevent, neutralize, or reduce a Borreliainfection.

The term “combination” refers to two or more nucleic acid molecules ofthe invention, or two or more polypeptides of the invention. In someaspects, combinations of molecules of the invention are administered toprovide immunity or fight infection from at least four of the sixserotypes (1-6) of Borrelia described herein. In various aspects,combinations of two or three molecules or polypeptides of the inventionare used. In certain aspects, combinations of molecules of the inventionare administered to a subject to provide immunity from all six serotypes(1-6) of Borrelia described herein. The latter combination has beenshown to provide immunity to heterologous strains of Borrelia expressingOspA types not present in the combination of nucleic acid molecules orpolypeptides.

The term “combination vaccine” refers to a vaccine formulationcontaining more than one vaccine composition or more than one protectiveantigen to one or more diseases. The invention includes a combinationvaccine comprising OspA chimeric antigens against Lyme disease orBorrelia in addition to an antigen against one or more other diseases.In various aspects, one or more of the other diseases is a tick-bornedisease. In certain aspects, the other tick-borne disease is RockyMountain Spotted Fever, Babesiosis, Relapsing Fever, Colorado tickfever, Human monocytic ehrlichiosis (HME), Human granulocyticehrlichiosis (HGE), Southern Tick-Associated Rash Illness (STARI),Tularemia, Tick paralysis, Powassan encephalitis, Q fever, Crimean-Congohemorrhagic fever, Cytauxzoonosis, boutonneuse fever, or tick-borneencephalitis. In particular aspects, the invention includes acombination vaccine which comprises one or more vaccines, including atick-borne encephalitis vaccine, a Japanese encephalitis vaccine, and aRocky Mountain Spotted Fever vaccine. In some aspects, the combinationvaccine comprises vaccine compositions that have a seasonal immunizationschedule compatible with immunization against Borrelia infection or Lymedisease. In more particular aspects, combination vaccines are useful inthe prevention of multiple diseases for use in geographical locationswhere these diseases are prevalent.

The term “Borrelia” refers to a species of Gram negative bacteria of thespirochete class of the genus Borrelia. In one aspect, “Borreliaburgdorferi sensu lato (s.l.)” refers to Borrelia burgdorferi in thewider sense. Almost all cases of Lyme disease or Borreliosis are causedby one of three genospecies, Borrelia afzelii, Borrelia garinii andBorrelia burgdorferi sensu stricto (s.s.), which refers to B.burgdorferi in the stricter sense). OspA serotypes of Borrelia correlatewith species; serotype 1 corresponds to B. burgdorferi s.s., serotype 2corresponds to B. afzelii and serotypes 3 to 7 correspond to B. garinii.In various aspects, the immunogenic or vaccine compositions of theinvention also provide protection against other species of Borreliaincluding, but not limited to, Borrelia japonica, Borrelia andersonii,Borrelia bissettii, Borrelia sinica, Borrelia turdi, Borrelia tanukii,Borrelia valaisiana, Borrelia lusitaniae, Borrelia spielmanii, Borreliamiyamotoi or Borrelia lonestar.

A “subject” is given its conventional meaning of a non-plant,non-protist living being. In most aspects, the subject is an animal. Inparticular aspects, the animal is a mammal. In more particular aspects,the mammal is a human. In other aspects, the mammal is a pet orcompanion animal, a domesticated farm animal, or a zoo animal. Incertain aspects, the mammal is a cat, dog, horse, or cow. In variousother aspects, the mammal is a deer, mouse, chipmunk, squirrel, opossum,or raccoon.

Lyme Disease (Borreliosis or Lyme Borreliosis)

In some aspects, the invention includes chimeric OspA molecules andcompositions comprising these molecules in the prevention of Lymedisease or Borrelia infection. Lyme Disease is also known in the art asBorreliosis or Lyme Borreliosis and, therefore, all of these terms areincluded in the invention. Likewise, the invention includes methods ofpreventing or treating Lyme disease comprising administering thechimeric OspA molecules described herein. Lyme disease, or borreliosis,is an infectious disease caused by at least three species ofGram-negative spirochetal bacteria belonging to the genus Borrelia.There are at least 13 Borrelia species which have been discovered, threeof which are known to be Lyme-related. The Borrelia species that causeLyme disease are collectively known as Borrelia burgdorferi sensu lato,and show a great deal of genetic diversity. The group Borreliaburgdorferi sensu lato is made up of three closely-related species thatare probably responsible for the large majority of cases. Borreliaburgdorferi sensu stricto is the main cause of Lyme disease in theUnited States (but it is also present in Europe), whereas Borreliaafzelii and Borrelia garinii cause most European cases. Some studieshave also proposed that Borrelia species (e.g. Borrelia bissettii,Boreffia spielmanii, Borrellia lusitaniae, and Borrelia valaisiana) maysometimes infect humans. Although these species do not seem to beimportant causes of disease, immunogenic protection against thesespecies is also include in the invention.

Lyme disease is the most common tick-borne disease in the NorthernHemisphere. The disease is named after the village of Lyme, Connecticutwhere a number of cases were identified in 1975. Borrelia is transmittedto humans by the bite of infected ticks belonging to a few species ofthe genus Ixodes (“hard ticks”). Early symptoms, in some instances,include fever, headache, fatigue, depression, and a characteristiccircular skin rash called erythema migrans. Left untreated, latersymptoms can often involve the joints, heart, and central nervoussystem. In most cases, the infection and its symptoms are eliminated byantibiotics, especially if the illness is treated early. However, late,delayed, or inadequate treatment can lead to the more serious symptoms,which can be disabling and difficult to treat. Occasionally, symptomssuch as arthritis persist after the infection has been eliminated byantibiotics.

Some groups have argued that “chronic” Lyme disease is responsible for arange of medically unexplained symptoms beyond the recognized symptomsof late Lyme disease, and that additional, long-term antibiotictreatments are needed. However, long-term treatment is controversial andthe dispute regarding such treatment has led to legal action overtreatment guidelines.

Lyme disease is classified as a zoonosis, as it is transmitted to humansfrom a natural reservoir which includes rodents and birds by ticks thatfeed on both sets of hosts. Hard-bodied ticks of the genus Ixodes arethe main vectors of Lyme disease. Most human infections are caused byticks in the nymphal stage, as the nymphal ticks are very small and mayfeed for long periods of time undetected. Tick bites often go unnoticedbecause of the small size of the tick in its nymphal stage, as well astick secretions that prevent the host from feeling any itch or pain fromthe bite.

Lyme disease is diagnosed clinically based on symptoms, objectivephysical findings (such as erythema migrans, facial palsy, orarthritis), a history of possible exposure to infected ticks, as well asserological blood tests. Approximately half of the patients with Lymedisease will develop the characteristic bulls-eye rash, but many may notrecall a tick bite. Laboratory testing is not recommended for personswho do not have symptoms of Lyme disease.

Because of the difficulty in culturing Borrelia bacteria in thelaboratory, diagnosis of Lyme disease is typically based on the clinicalexam findings and a history of exposure to endemic Lyme areas. TheErythema migrans (EM) rash, which only occurs in about 50% of all cases,is considered sufficient to establish a diagnosis of Lyme disease evenwhen serologic blood tests are negative. Serological testing can be usedto support a clinically suspected case but is not diagnostic by itself.Diagnosis of late-stage Lyme disease is often difficult because of themulti-faceted appearance which can mimic symptoms of many otherdiseases. For this reason, a reviewer called Lyme the new “greatimitator.” Lyme disease, in some instances, is misdiagnosed as multiplesclerosis, rheumatoid arthritis, fibromyalgia, chronic fatigue syndrome(CFS), lupus, or other autoimmune and neurodegenerative diseases. Thus,there is a great need in the art for a vaccine to prevent or treat Lymedisease.

Outer Surface Protein A (OspA) of Borrelia

In various aspects, the invention includes chimeric OspA molecules ofBorrelia and compositions comprising these molecules in the preventionand treatment of Lyme disease or Borrelia infection. Several Borreliaouter surface proteins have been identified over the past decade thatare up-regulated by temperature- and/or mammalian host-specific signalsas this spirochete is transmitted from ticks to mammals.

The major outer surface protein, OspA, of Borrelia burgdorferi is alipoprotein of particular interest because of its potential as a vaccinecandidate. Serotypic and genetic analysis of OspA from both European andNorth American strains of Borrelia have demonstrated antigenic andstructural heterogeneities. OspA is described in published PCT patentapplication WO 92/14488, in Jiang et al. (Clin. Diagn. Lab. Immunol. 1:406-12, 1994) and is known in the art. Osp A has been shown to induceprotective immunity in mouse, hamster and dog challenge studies.Clinical trials in humans have shown the formulations of OspA to be safeand immunogenic in humans (Keller et al., JAMA (1994) 271:1764 1768).

While OspA is expressed in the vast majority of clinical isolates ofBorrelia burgdorferi from North America, a different picture has emergedfrom examination of the clinical Borrelia isolates in Europe. In Europe,Lyme disease is mainly caused by three genospecies of Borrelia, namelyB. burgdorferi, B. garinii and B. afzelii. The invention is directed tochimeric OspA molecules that provide protective immunity against allgenospecies of Borrelia. The invention describes the design andsynthesis of three chimeric OspA genes that encode for three distinctlipidated OspA molecules that share common features. Each generepresents two OspA serotypes and the genes were designed to encodestable OspA molecules that are safe and highly immunogenic, and afford asubject protection against infection with B. burgdorferi sensu lato(s.l.). The invention also describes three original chimeric OspA geneswithout mutations and without codon optimization that encode threedistinct lipidated OspA molecules that share common features. Each generepresents two OspA serotypes and encode molecules that afford a subjectprotection against infection with B. burgdorferi sensu lato (s.l.).

Seven principal OspA serotypes have been recognized among Europeanisolates (designated serotypes 1 to 7, Wilske et al., J. Clin.Microbiol. 31:340-50, 1993). OspA serotypes correlate with species;serotype 1 corresponds to B. burgdorferi s.s., serotype 2 corresponds toB. afzelii and serotypes 3 to 7 correspond to B. garinii.Epidemiological studies of European Borrelia isolates indicate that avaccine based on OspA types 1, 2, 3, 4, 5 and 6 would providetheoretical coverage in Europe of 98.1% of Lyme disease and cover 96.7%of invasive disease isolates. The invention provides six chimeric OspAnucleic acid molecules (SEQ ID NOS: 1, 3, and 5, and SEQ ID NOS: 168,170, and 172) and six chimeric OspA polypeptide molecules (SEQ ID NOS:2, 4, and 6, and SEQ ID NOS: 169, 171, and 173) that can provideprotective immunity against all six serotypes 1-6. Six synthetic OspAgenes were designed to encode OspA molecules with the protectiveepitopes from OspA serotypes 1 and 2 (lipB sOspA 1/2²⁵¹ (SEQ ID NOS: 1(nucleic acid) and 2 (amino acid) and orig sOspA 1/2 (SEQ ID NOS: 168(nucleic acid) and 169 (amino acid)); OspA serotypes 6 and 4 (lipB sOspA6/4 (SEQ ID NOS: 3 (nucleic acid) and 4 (amino acid) and orig sOspA 6/4(SEQ ID NOS: 170 (nucleic acid) and 171 (amino acid)); and OspAserotypes 5 and 3 (lipB sOspA 5/3 (SEQ ID NOS: 5 (nucleic acid) and 6(amino acid) and orig sOspA 5/3 (SEQ ID NOS: 172 (nucleic acid) and 173(amino acid)). The chimeric OspA genes were made using syntheticoverlapping oligonucleotides. These recombinant proteins are, in certainaspects, produced at high yield and purity and, in various aspects,manipulated to maximize desirable activities and minimize undesirableones.

Chimeric OspA Nucleic Acid Molecules and Polypeptide Molecules

In various aspects, the invention includes chimeric OspA nucleic acidand polypeptide molecules of Borrelia. The OspA nucleic acids of theinvention include a nucleic acid molecule comprising, consistingessentially of, or consisting of a nucleotide sequence as set forth inSEQ ID NO: 1 (lipB sOspA 1/2²⁵¹), SEQ ID NO: 3 (lipB sOspA 6/4), SEQ IDNO: 5 (lipB sOspA 5/3), SEQ ID NO: 7 (sOspA 1/2²⁵¹), SEQ ID NO: 9 (sOspA6/4), SEQ ID NO: 11 (sOspA 5/3), SEQ ID NO: 168 (orig sOspA 1/2), SEQ IDNO: 170 (orig sOspA 6/4), or SEQ ID NO: 172 (orig sOspA 5/3), or anucleotide sequence encoding the polypeptide as set forth in SEQ ID NO:2 (lipB sOspA 1/2²⁵¹), SEQ ID NO: 4 (lipB sOspA 6/4), SEQ ID NO: 6 (lipBsOspA 5/3), SEQ ID NO: 8 (sOspA 1/2²⁵¹), SEQ ID NO: 10 (sOspA 6/4), SEQID NO: 12 (sOspA 5/3), SEQ ID NO: 169 (orig sOspA 1/2), SEQ ID NO: 171(orig sOspA 6/4), or SEQ ID NO: 173 (orig sOspA 5/3).

The nucleic acid sequences of SEQ ID NOS: 7, 9, and 11 lack the nucleicacid sequence encoding the lipB leader sequence (MRLLIGFALALALIG (SEQ IDNO: 13). In addition, the nucleic acid sequences of SEQ ID NOS: 7, 9,and 11 encode a methionine residue at the amino terminus of SEQ ID NOS:8, 10, and 12 in place of the cysteine residue present at the carboxyterminus of the lipB leader sequence in SEQ ID NOS: 2, 4, and 6. SEQ IDNOS: 1, 3, and 5 are lipB sOspA polynucleotides, and SEQ ID NOS: 2, 4,and 6 are lipB sOspA polypeptides.

In some aspects, the invention includes original (“orig”) chimeric OspAnucleic acid and polypeptide molecules of Borrelia without mutations andwithout codon optimization. The OspA nucleic acids of the invention,therefore, include a nucleic acid molecule comprising, consistingessentially of, or consisting of a nucleotide sequence as set forth inSEQ ID NO: 168 (orig sOspA 1/2), SEQ ID NO: 170 (orig sOspA 6/4), or SEQID NO: 172 (orig sOspA 5/3), or a nucleotide sequence encoding thepolypeptide as set forth in SEQ ID NO: 169 (orig sOspA 1/2), SEQ ID NO:171 (orig sOspA 6/4), or SEQ ID NO: 173 (orig sOspA 5/3).

Sequence identification numbers for DNA and amino acid sequences for thechimeric OspA molecules are set out in Table 1 below.

TABLE 1  Chimeric OspA DNA and Amino Acid Sequences Amino DNA AcidComplementary SEQ ID SEQ ID Strand Sequence NO: NO: SEQ ID NO:lipB sOspA 1/2²⁵¹ 1 2 48 lipB sOspA 6/4 3 4 49 lipB sOspA 5/3 5 6 50sOspA 1/2²⁵¹ 7 8 56 sOspA 6/4 9 10 57 sOspA 5/3 11 12 58 Orig sOspA 1/2168 169 Orig sOspA 6/4 170 171 Orig sOspA 5/3 172 173 lipB sOspA 1/2²⁵¹Amino Acid Sequence (SEQ ID NO: 2)MRLLIGFALALALIGCAQKGAESIGSVSVDLPGEMKVLVSKEKDKNGKYDLIATVDKLELKGTSDKNNGSGVLEGVKTNKSKVKLTISDDLGQTTLEVEKEDGKTLVSKKVTSKDKSSTEEKENEKGEVSEKIITMADGTRLEYTGIKSDGTGKAKYVLKNFTLEGKVANDKTTLEVKEGTVTLSMNISKSGEVSVELNDTDSSAATKKTAAWNSKTSTLTISVNSKKTTQLVFTKQDTITVQKYDSAGTNLEGTAVEIKTLDELKNALKDNA Sequence  (SEQ ID NO: 1)catatgcgtctgttgatcggctttgctctggcgctggctctgatcggctgcgcacagaaaggtgctgagtctattggttccgtttctgtagatctgcccggtgaaatgaaggttctggtgagcaaagaaaaagacaagaacggcaagtacgatctcatcgcaaccgtcgacaagctggagctgaaaggtacttctgataaaaacaacggctctggtgtgctggagggcgtcaaaactaacaagagcaaagtaaagcttacgatctctgacgatctcggtcagaccacgctggaagttttcaaagaggatggcaagaccctcgtgtccaaaaaagtaacttccaaagacaagtcctctacggaagaaaaattcaacgaaaaaggtgaggtgtctgaaaagatcatcaccatggcagacggcacccgtcttgaatacaccggtattaaaagcgatggtaccggtaaagcgaaatatgttctgaaaaacttcactctggaaggcaaagtggctaatgataaaaccaccttggaagtcaaggaaggcaccgttactctgagcatgaatatctccaaatctggtgaagtttccgttgaactgaacgacactgacagcagcgctgcgactaaaaaaactgcagcgtggaattccaaaacttctactttaaccattagcgttaacagcaaaaaaactacccagctggtgttcactaaacaagacacgatcactgtgcagaaatacgactccgcaggcaccaacttagaaggcacggcagtcgaaattaaaacccttgatgaactgaaaaacgcgctgaaataagctgagcggatccComplementary Strand  (SEQ ID NO: 48)catatgcgtctgttgatcggctttgctttggcgctggctttaatcggctgtgcacagaaaggtgctgagtctattggttccgtttctgtagatctgcccgggggtatgaaagttctggtaagcaaagaaaaagacaaaaacggtaaatacagcctgatggcaaccgtagaaaagctggagcttaaaggcacttctgataaaaacaacggttctggcaccctggaaggtgaaaaaactaacaaaagcaaagtaaagcttactattgctgaggatctgagcaaaaccacctttgaaatcttcaaagaagatggcaaaactctggtatctaaaaaagtaaccctgaaagacaagtcttctaccgaagaaaaattcaacgaaaagggtgaaatctctgaaaaaactatcgtaatggcaaatggtacccgtctggaatacaccgacatcaaaagcgataaaaccggcaaagctaaatacgttctgaaagactttactctggaaggcactctggctgctgacggcaaaaccactctgaaagttaccgaaggcactgttactctgagcatgaacatttctaaatccggcgaaatcaccgttgcactggatgacactgactctagcggcaataaaaaatccggcacctgggattctgatacttctactttaaccattagcaaaaacagccagaaaactaaacagctggtattcaccaaagaaaacactatcaccgtacagaactataaccgtgcaggcaatgcgctggaaggcagcccggctgaaattaaagatctggcagagctgaaagccgctttgaaataagctgagcggatcclipB sOspA 6/4 Amino Acid Sequence  (SEQ ID NO: 4)MRLLIGFALALALIGCAQKGAESIGSVSVDLPGGMTVLVSKEKDKNGKYSLEATVDKLELKGTSDKNNGSGTLEGEKTNKSKVKLTIADDLSQTKFEIFKEDAKTLVSKKVTLKDKSSTEEKFNEKGETSEKTIVMANGTRLEYTDIKSDGSGKAKYVLKDFTLEGTLAADGKTTLKVTEGTVVLSMNILKSGEITVALDDSDTTQATKKTGKWDSNTSTLTISVNSKKTKNIVFTKEDTITVQKYDSAGTNLEGNAVEIKTLDELKNALKDNA Sequence  (SEQ ID NO: 3)catatgcgtctgttgatcggctttgctctggcgctggctctgatcggctgcgcacagaaaggtgctgagtctattggttccgtttctgtagatctgcccggtggcatgaccgttctggtcagcaaagaaaaagacaaaaacggtaaatacagcctcgaggcgaccgtcgacaagcttgagctgaaaggcacctctgataaaaacaacggttccggcaccctggaaggtgaaaaaactaacaaaagcaaagtgaaactgaccattgctgatgacctcagccagaccaaattcgaaattttcaaagaagatgccaaaaccttagtatccaaaaaagtgaccctgaaagacaagtcctctaccgaagaaaaattcaacgaaaagggtgaaacctctgaaaaaaccatcgtaatggcaaatggtacccgtctggaatacaccgacatcaaaagcgatggctccggcaaagccaaatacgttctgaaagacttcaccctggaaggcaccctcgctgccgacggcaaaaccaccttgaaagttaccgaaggcactgttgttttaagcatgaacatcttaaaatccggtgaaatcaccgttgcgctggatgactctgacaccactcaggccactaaaaaaaccggcaaatgggattctaacacttccactctgaccatcagcgtgaattccaaaaaaactaaaaacatcgtgttcaccaaagaagacaccatcaccgtccagaaatacgactctgcgggcaccaacctcgaaggcaacgcagtcgaaatcaaaaccctggatgaactgaaaaacgctctgaaataagctgagcggatccComplementary Strand  (SEQ ID NO: 49)ggatccgctcagcttatttcagcgcgtttttcagttcatcaagggttttaatttcgactgccgtgccttctaagttggtgcctgcggagtcgtatttctgcacagtgatcgtgtcttgtttagtgaacaccagctgggtagtttttttgctgttaacgctaatggttaaagtagaagttttggaattccacgctgcagtttttttagtcgcagcgctgctgtcagtgtcgttcagttcaacggaaacttcaccagatttggagatattcatgctcagagtaacggtgccttccttgacttccaaggtggttttatcattagccactttgccttccagagtgaagtttttcagaacatatttcgctttaccggtaccatcgcttttaataccggtgtattcaagacgggtgccgtctgccatggtgatgatcttttcagacacctcacctttttcgttgaatttttcttccgtagaggacttgtctttggaagttacttttttggacacgagggtcttgccatcctctttgaaaacttccagcgtggtctgaccgagatcgtcagagatcgtaagctttactttgctcttgttagttttgacgccctccagcacaccagagccgttgtttttatcagaagtacctttcagctccagcttgtcgacggttgcgatgagatcgtacttgccgttcttgtctttttctttgctcaccagaaccttcatttcaccgggcagatctacagaaacggaaccaatagactcagcacctttctgtgcgcagccgatcagagccagcgccagagcaaagccgatcaacagacgcatatglipB sOspA 5/3 Amino Acid Sequence  (SEQ ID NO: 6)MRLLIGFALALALIGCAQKGAESIGSVSVDLPGGMKVLVSKEKDKNGKYSLMATVEKLELKGTSDKNNGSGTLEGEKTNKSKVKLTIAEDLSKTTFEIFKEDGKTLVSKKVTLKDKSSTEEKENEKGEISEKTIVMANGTRLEYTDIKSDKTGKAKYVLKDFTLEGTLAADGKTTLKVTEGTVTLSMNISKSGEITVALDDTDSSGNKKSGTWDSDTSTLTISKNSQKTKQLVETKENTITVQNYNRAGNALEGSPAEIKDLAELKAALKDNA Sequence  (SEQ ID NO: 5)catatgcgtctgttgatcggctttgctttggcgctggctttaatcggctgtgcacagaaaggtgctgagtctattggttccgtttctgtagatctgcccgggggtatgaaagttctggtaagcaaagaaaaagacaaaaacggtaaatacagcctgatggcaaccgtagaaaagctggagcttaaaggcacttctgataaaaacaacggttctggcaccctggaaggtgaaaaaactaacaaaagcaaagtaaagcttactattgctgaggatctgagcaaaaccacctttgaaatcttcaaagaagatggcaaaactctggtatctaaaaaagtaaccctgaaagacaagtcttctaccgaagaaaaattcaacgaaaagggtgaaatctctgaaaaaactatcgtaatggcaaatggtacccgtctggaatacaccgacatcaaaagcgataaaaccggcaaagctaaatacgttctgaaagactttactctggaaggcactctggctgctgacggcaaaaccactctgaaagttaccgaaggcactgttactctgagcatgaacatttctaaatccggcgaaatcaccgttgcactggatgacactgactctagcggcaataaaaaatccggcacctgggattctgatacttctactttaaccattagcaaaaacagccagaaaactaaacagctggtattcaccaaagaaaacactatcaccgtacagaactataaccgtgcaggcaatgcgctggaaggcagcccggctgaaattaaagatctggcagagctgaaagccgctttgaaataagctgagcggatccComplementary Strand  (SEQ ID NO: 50)ggatccgctcagcttatttcagagcgtttttcagttcatccagggttttgatttcgactgcgttgccttcgaggttggtgcccgcagagtcgtatttctggacggtgatggtgtcttctttggtgaacacgatgtttttagtttttttggaattcacgctgatggtcagagtggaagtgttagaatcccatttgccggtttttttagtggcctgagtggtgtcagagtcatccagcgcaacggtgatttcaccggattttaagatgttcatgcttaaaacaacagtgccttcggtaactttcaaggtggttttgccgtcggcagcgagggtgccttccagggtgaagtctttcagaacgtatttggctttgccggagccatcgcttttgatgtcggtgtattccagacgggtaccatttgccattacgatggttttttcagaggtttcacccttttcgttgaatttttcttcggtagaggacttgtctttcagggtcacttttttggatactaaggttttggcatcttctttgaaaatttcgaatttggtctggctgaggtcatcagcaatggtcagtttcactttgcttttgttagttttttcaccttccagggtgccggaaccgttgtttttatcagaggtgcctttcagctcaagcttgtcgacggtcgcctcgaggctgtatttaccgtttttgtctttttctttgctgaccagaacggtcatgccaccgggcagatctacagaaacggaaccaatagactcagcacctttctgtgcgcagccgatcagagccagcgccagagcaaagccgatcaacagacgcatatgsOspA 1/2²⁵¹ Amino Acid Sequence  (SEQ ID NO: 8)MAQKGAESIGSVSVDLPGEMKVLVSKEKDKNGKYDLIATVDKLELKGTSDKNNGSGVLEGVKTNKSKVKLTISDDLGQTTLEVFKEDGKTLVSKKVTSKDKSSTEEKFNEKGEVSEKIITMADGTRLEYTGIKSDGTGKAKYVLKNFTLEGKVANDKTTLEVKEGTVTLSMNISKSGEVSVELNDTDSSAATKKTAAWNSKTSTLTISVNSKKTTQLVFTKQDTITVQKYDSAGTNLEGTAVEIKTLDELKNALK DNA Sequence (SEQ ID NO: 7)catatggcacagaaaggtgctgagtctattggttccgtttctgtagatctgcccggtgaaatgaaggttctggtgagcaaagaaaaagacaagaacggcaagtacgatctcatcgcaaccgtcgacaagctggagctgaaaggtacttctgataaaaacaacggctctggtgtgctggagggcgtcaaaactaacaagagcaaagtaaagcttacgatctctgacgatctcggtcagaccacgctggaagttttcaaagaggatggcaagaccctcgtgtccaaaaaagtaacttccaaagacaagtcctctacggaagaaaaattcaacgaaaaaggtgaggtgtctgaaaagatcatcaccatggcagacggcacccgtcttgaatacaccggtattaaaagcgatggtaccggtaaagcgaaatatgttctgaaaaacttcactctggaaggcaaagtggctaatgataaaaccaccttggaagtcaaggaaggcaccgttactctgagcatgaatatctccaaatctggtgaagtttccgttgaactgaacgacactgacagcagcgctgcgactaaaaaaactgcagcgtggaattccaaaacttctactttaaccattagcgttaacagcaaaaaaactacccagctggtgttcactaaacaagacacgatcactgtgcagaaatacgactccaacggcaccaacttagaaggcacggcagtcgaaattaaaacccttgatgaactgaaaaacgcgctgaaataagctgagcggatcc Complementary Strand  (SEQ ID NO: 56)gtataccgtgtctttccacgactcagataaccaaggcaaagacatctagacgggccactttacttccaagaccactcgtttctttttctgttcttgccgttcatgctagagtagcgttggcagctgttcgacctcgactttccatgaagactatttttgttgccgagaccacacgacctcccgcagttttgattgttctcgtttcatttcgaatgctagagactgctagagccagtctggtgcgaccttcaaaagtttctcctaccgttctgggagcacaggttttttcattgaaggtttctgttcaggagatgccttctttttaagttgctttttccactccacagacttttctagtagtggtaccgtctgccgtgggcagaacttatgtggccataattttcgctaccatggccatttcgctttatacaagactttttgaagtgagaccttccgtttcaccgattactattttggtggaaccttcagttccttccgtggcaatgagactcgtacttatagaggtttagaccacttcaaaggcaacttgacttgctgtgactgtcgtcgcgacgctgatttttttgacgtcgcaccttaaggttttgaagatgaaattggtaatcgcaattgtcgtttttttgatgggtcgaccacaagtgatttgttctgtgctagtgacacgtctttatgctgaggttgccgtggttgaatcttccgtgccgtcagctttaattttgggaactacttgactttttgcgcgactttattcgactcgcctagg sOspA 6/4 Amino Acid Sequence  (SEQ ID NO: 10)MAQKGAESIGSVSVDLPGGMTVLVSKEKDKNGKYSLEATVDKLELKGTSDKNNGSGTLEGEKTNKSKVKLTIADDLSQTKFEIFKEDAKTLVSKKVTLKDKSSTEEKFNEKGETSEKTIVMANGTRLEYTDIKSDGSGKAKYVLKDFTLEGTLAADGKTTLKVTEGTVVLSMNILKSGEITVALDDSDTTQATKKTGKWDSNTSTLTISVNSKKTKNIVFTKEDTITVQKYDSAGTNLEGNAVEIKTLDELKNALK DNA Sequence (SEQ ID NO: 9)catatggcacagaaaggtgctgagtctattggttccgtttctgtagatctgcccggtggcatgaccgttctggtcagcaaagaaaaagacaaaaacggtaaatacagcctcgaggcgaccgtcgacaagcttgagctgaaaggcacctctgataaaaacaacggttccggcaccctggaaggtgaaaaaactaacaaaagcaaagtgaaactgaccattgctgatgacctcagccagaccaaattcgaaattttcaaagaagatgccaaaaccttagtatccaaaaaagtgaccctgaaagacaagtcctctaccgaagaaaaattcaacgaaaagggtgaaacctctgaaaaaaccatcgtaatggcaaatggtacccgtctggaatacaccgacatcaaaagcgatggctccggcaaagccaaatacgttctgaaagacttcaccctggaaggcaccctcgctgccgacggcaaaaccaccttgaaagttaccgaaggcactgttgttttaagcatgaacatcttaaaatccggtgaaatcaccgttgcgctggatgactctgacaccactcaggccactaaaaaaaccggcaaatgggattctaacacttccactctgaccatcagcgtgaattccaaaaaaactaaaaacatcgtgttcaccaaagaagacaccatcaccgtccagaaatacgactctgcgggcaccaacctcgaaggcaacgcagtcgaaatcaaaaccctggatgaactgaaaaacgctctgaaataagctgagcggatcc Complementary Strand  (SEQ ID NO: 57)gtataccgtgtctttccacgactcagataaccaaggcaaagacatctagacgggccaccgtactggcaagaccagtcgtttctttttctgtttttgccatttatgtcggagctccgctggcagctgttcgaactcgactttccgtggagactatttttgttgccaaggccgtgggaccttccacttttttgattgttttcgtttcactttgactggtaacgactactggagtcggtctggtttaagctttaaaagtttcttctacggttttggaatcataggttttttcactgggactttctgttcaggagatggcttctttttaagttgcttttcccactttggagacttttttggtagcattaccgtttaccatgggcagaccttatgtggctgtagttttcgctaccgaggccgtttcggtttatgcaagactttctgaagtgggaccttccgtgggagcgacggctgccgttttggtggaactttcaatggcttccgtgacaacaaaattcgtacttgtagaattttaggccactttagtggcaacgcgacctactgagactgtggtgagtccggtgatttttttggccgtttaccctaagattgtgaaggtgagactggtagtcgcacttaaggtttttttgatttttgtagcacaagtggtttcttctgtggtagtggcaggtctttatgctgagacgcccgtggttggagcttccgttgcgtcagctttagttttgggacctacttgactttttgcgagactttattcgactcgcctagg sOspA 5/3 Amino Acid Sequence  (SEQ ID NO: 12)MAQKGAESIGSVSVDLPGGMKVLVSKEKDKNGKYSLMATVEKLELKGTSDKNNGSGTLEGEKTNKSKVKLTIAEDLSKTTFEIFKEDGKTLVSKKVTLKDKSSTEEKENEKGEISEKTIVMANGTRLEYTDIKSDKTGKAKYVLKDFTLEGTLAADGKTTLKVTEGTVTLSMNISKSGEITVALDDTDSSGNKKSGTWDSDTSTLTISKNSQKTKQLVFTKENTITVQNYNRAGNALEGSPAEIKDLAELKAALK DNA Sequence (SEQ ID NO: 11)catatggcacagaaaggtgctgagtctattggttccgtttctgtagatctgcccgggggtatgaaagttctggtaagcaaagaaaaagacaaaaacggtaaatacagcctgatggcaaccgtagaaaagctggagcttaaaggcacttctgataaaaacaacggttctggcaccctggaaggtgaaaaaactaacaaaagcaaagtaaagcttactattgctgaggatctgagcaaaaccacctttgaaatcttcaaagaagatggcaaaactctggtatctaaaaaagtaaccctgaaagacaagtcttctaccgaagaaaaattcaacgaaaagggtgaaatctctgaaaaaactatcgtaatggcaaatggtacccgtctggaatacaccgacatcaaaagcgataaaaccggcaaagctaaatacgttctgaaagactttactctggaaggcactctggctgctgacggcaaaaccactctgaaagttaccgaaggcactgttactctgagcatgaacatttctaaatccggcgaaatcaccgttgcactggatgacactgactctagcggcaataaaaaatccggcacctgggattctgatacttctactttaaccattagcaaaaacagccagaaaactaaacagctggtattcaccaaagaaaacactatcaccgtacagaactataaccgtgcaggcaatgcgctggaaggcagcccggctgaaattaaagatctggcagagctgaaagccgctttgaaataagctgagcggatcc Complementary Strand  (SEQ ID NO: 58)gtataccgtgtctttccacgactcagataaccaaggcaaagacatctagacgggcccccatactttcaagaccattcgtttctttttctgtttttgccatttatgtcggactaccgttggcatcttttcgacctcgaatttccgtgaagactatttttgttgccaagaccgtgggaccttccacttttttgattgttttcgtttcatttcgaatgataacgactcctagactcgttttggtggaaactttagaagtttcttctaccgttttgagaccatagattttttcattgggactttctgttcagaagatggcttctttttaagttgcttttcccactttagagacttttttgatagcattaccgtttaccatgggcagaccttatgtggctgtagttttcgctattttggccgtttcgatttatgcaagactttctgaaatgagaccttccgtgagaccgacgactgccgttttggtgagactttcaatggcttccgtgacaatgagactcgtacttgtaaagatttaggccgctttagtggcaacgtgacctactgtgactgagatcgccgttattttttaggccgtggaccctaagactatgaagatgaaattggtaatcgtttttgtcggtcttttgatttgtcgaccataagtggtttcttttgtgatagtggcatgtcttgatattggcacgtccgttacgcgaccttccgtcgggccgactttaatttctagaccgtctcgactttcggcgaaactttattcgactcgcctagg Orig sOspA 1/2 Amino Acid Sequence  (SEQ ID NO: 169)MKKYLLGIGLILALIACKQNVSSLDEKNSVSVDLPGEMKVLVSKEKNKDGKYDLIATVDKLELKGTSDKNNGSGVLEGVKADKSKVKLTISDDLGQTTLEVFKEDGKTLVSKKVTSKDKSSTEEKFNEKGEVSEKIITRADGTRLEYTGIKSDGSGKAKEVLKNFTLEGKVANDKVTLEVKEGTVTLSKNISKSGEVSVELNDTDSSAATKKTAAWNSKTSTLTISVNSKKTTQLVFTKQDTITVQKYDSAGTNLEGTAVEIKTLDELKNALK DNA Sequence  (SEQ ID NO: 168)atgaaaaaatatttattgggaataggtctaatattagccttaatagcatgtaagcaaaatgttagcagccttgacgagaaaaacagcgtttcagtagatttgcctggtgaaatgaaagttcttgtaagcaaagaaaaaaacaaagacggcaagtacgatctaattgcaacagtagacaagcttgagcttaaaggaacttctgataaaaacaatggatctggagtacttgaaggcgtaaaagctgacaaaagtaaagtaaaattaacaatttctgacgatctaggtcaaaccacacttgaagttttcaaagaagatggcaaaacactagtatcaaaaaaagtaacttccaaagacaagtcatcaacagaagaaaaattcaatgaaaaaggtgaagtatctgaaaaaataataacaagagcagacggaaccagacttgaatacacaggaattaaaagcgatggatctggaaaagctaaagaggttttaaaaaactttactcttgaaggaaaagtagctaatgataaagtaacattggaagtaaaagaaggaaccgttactttaagtaaaaatatttcaaaatctggggaagtttcagttgaacttaatgacactgacagtagtgctgctactaaaaaaactgcagcttggaattcaaaaacttctactttaacaattagtgttaacagcaaaaaaactacacaacttgtgtttactaaacaagacacaataactgtacaaaaatacgactccgcaggtaccaatttagaaggcacagcagtcgaaattaaaacacttgatgaacttaaaaacgctttaaaatag Orig sOspA 6/4 Amino Acid Sequence  (SEQ ID NO: 171)MKKYLLGIGLILALIACKQNVSTLDEKNSVSVDLPGGMTVLVSKEKDKDGKYSLEATVDKLELKGTSDKNNGSGTLEGEKTDKSKVKLTIADDLSQTKFEIFKEDAKTLVSKKVTLKDKSSTEEKFNEKGETSEKTIVRANGTRLEYTDIKSDGSGKAKEVLKDFTLEGTLAADGKTTLKVTEGTVVLSKNILKSGEITVALDDSDTTQATKKTGKWDSNTSTLTISVNSKKTKNIVFTKEDTITVQKYDSAGTNLEGNAVEIKTLDELKNALK DNA Sequence  (SEQ ID NO: 170)atgaaaaaatatttattgggaataggtctaatattagccttaatagcatgtaagcaaaatgttagcacgcttgatgaaaaaaatagcgtttcagtagatttacctggtggaatgacagttcttgtaagtaaagaaaaagacaaagacggtaaatacagtctagaggcaacagtagacaagcttgagcttaaaggaacttctgataaaaacaacggttctggaacacttgaaggtgaaaaaactgacaaaagtaaagtaaaattaacaattgctgatgacctaagtcaaactaaatttgaaattttcaaagaagatgccaaaacattagtatcaaaaaaagtaacccttaaagacaagtcatcaacagaagaaaaattcaacgaaaagggtgaaacatctgaaaaaacaatagtaagagcaaatggaaccagacttgaatacacagacataaaaagcgatggatccggaaaagctaaagaagttttaaaagactttactcttgaaggaactctagctgctgacggcaaaacaacattgaaagttacagaaggcactgttgttttaagcaagaacattttaaaatccggagaaataacagttgcacttgatgactctgacactactcaggctactaaaaaaactggaaaatgggattcaaatacttccactttaacaattagtgtgaatagcaaaaaaactaaaaacattgtatttacaaaagaagacacaataacagtacaaaaatacgactcagcaggcaccaatctagaaggcaacgcagtcgaaattaaaacacttgatgaacttaaaaacgctttaaaataa Orig sOspA 5/3 Amino Acid Sequence  (SEQ ID NO: 173)MKKYLLGIGLILALIACKQNVSSLDEKNSVSVDLPGGMKVLVSKEKDKDGKYSLMATVEKLELKGTSDKNNGSGTLEGEKTDKSKVKLTIAEDLSKTTFEIFKEDGKTLVSKKVTLKDKSSTEEKFNEKGEISEKTIVRANGTRLEYTDIKSDKTGKAKEVLKDFTLEGTLAADGKTTLKVTEGTVTLSKNISKSGEITVALDDTDSSGNKKSGTWDSDTSTLTISKNSQKTKQLVFTKENTITVQNYNRAGNALEGSPAEIKDLAELKAALK DNA Sequence  (SEQ ID NO: 172)atgaaaaaatatttattgggaataggtctaatattagccttaatagcatgtaagcaaaatgttagcagccttgatgaaaaaaatagcgtttcagtagatttacctggtggaatgaaagttcttgtaagtaaagaaaaagacaaagatggtaaatacagtctaatggcaacagtagaaaagcttgagcttaaaggaacttctgataaaaacaacggttctggaacacttgaaggtgaaaaaactgacaaaagtaaagtaaaattaacaattgctgaggatctaagtaaaaccacatttgaaatcttcaaagaagatggcaaaacattagtatcaaaaaaagtaacccttaaagacaagtcatcaacagaagaaaaattcaacgaaaagggtgaaatatctgaaaaaacaatagtaagagcaaatggaaccagacttgaatacacagacataaaaagcgataaaaccggaaaagctaaagaagttttaaaagactttactcttgaaggaactctagctgctgacggcaaaacaacattgaaagttacagaaggcactgttactttaagcaagaacatttcaaaatccggagaaataacagttgcacttgatgacactgactctagcggcaataaaaaatccggaacatgggattcagatacttctactttaacaattagtaaaaacagtcaaaaaactaaacaacttgtattcacaaaagaaaacacaataacagtacaaaactataacagagcaggcaatgcgcttgaaggcagcccagctgaaattaaagatcttgcagagcttaaagccgctttaaaataa

The OspA polypeptides of the invention include a polypeptide comprising,consisting essentially of, or consisting of the amino acid sequence ofSEQ ID NO: 2 (lipB sOspA 1/2²⁵¹), SEQ ID NO: 4 (lipB sOspA 6/4), SEQ IDNO: 6 (lipB sOspA 5/3), SEQ ID NO: 8 (sOspA 1/2²⁵¹), SEQ ID NO: 10(sOspA 6/4), SEQ ID NO: 12 (sOspA 5/3), SEQ ID NO: 169 (orig sOspA 1/2),SEQ ID NO: 171 (orig sOspA 6/4), or SEQ ID NO: 173 (orig sOspA 5/3) andrelated polypeptides. Related polypeptides include OspA polypeptideanalogs, OspA polypeptide variants and OspA polypeptide derivatives. Insome aspects, an OspA polypeptide has an amino terminal methionineresidue, depending on the method by which they are prepared. In relatedaspects, the OspA polypeptide of the invention comprises OspA activity.

In one embodiment, related nucleic acid molecules comprise or consist ofa nucleotide sequence that is about 70 percent (70%) identical orsimilar to the nucleotide sequence as shown in SEQ ID NO: 1 (lipB sOspA1/2²⁵¹), SEQ ID NO: 3 (lipB sOspA 6/4), SEQ ID NO: 5 (lipB sOspA 5/3),SEQ ID NO: 7 (sOspA 1/2²⁵¹), SEQ ID NO: 9 (sOspA 6/4), SEQ ID NO: 11(sOspA 5/3), SEQ ID NO: 168 (orig sOspA 1/2), SEQ ID NO: 170 (orig sOspA6/4), or SEQ ID NO: 172 (orig sOspA 5/3), in certain aspects, comprise,consist essentially of, or consist of a nucleotide sequence encoding apolypeptide that is about 70 percent (70%) identical to the polypeptideas set forth in SEQ ID NO: 2 (lipB sOspA 1/2²⁵¹), SEQ ID NO: 4 (lipBsOspA 6/4), SEQ ID NO: 6 (lipB sOspA 5/3), SEQ ID NO: 8 (sOspA 1/2²⁵¹),SEQ ID NO: 10 (sOspA 6/4), SEQ ID NO: 12 (sOspA 5/3), SEQ ID NO: 169(orig sOspA 1/2), SEQ ID NO: 171 (orig sOspA 6/4), or SEQ ID NO: 173(orig sOspA 5/3). In various embodiments, the nucleotide sequences areabout 70 percent, or about 71, 72, 73, 74, 75, 76, 77, 78, or 79percent, or about 80 percent, or about 81, 82, 83, 84, 85, 86, 87, 88,or 89 percent, or about 90 percent, or about 91, 92, 93, 94, 95, 96, 97,98, or 99 percent identical to the nucleotide sequence as shown in SEQID NO: 1 (lipB sOspA 1/2²⁵¹), SEQ ID NO: 3 (lipB sOspA 6/4), SEQ ID NO:5 (lipB sOspA 5/3), SEQ ID NO: 7 (sOspA 1/2²⁵¹), SEQ ID NO: 9 (sOspA6/4), SEQ ID NO: 11 (sOspA 5/3), SEQ ID NO: 168 (orig sOspA 1/2), SEQ IDNO: 170 (orig sOspA 6/4), or SEQ ID NO: 172 (orig sOspA 5/3), or thenucleotide sequences encode a polypeptide that is about 70 percent, orabout 71, 72, 73, 74, 75, 76, 77, 78, or 79 percent, or about 80percent, or about 81, 82, 83, 84, 85, 86, 87, 88, or 89 percent, orabout 90 percent, or about 91, 92, 93, 94, 95, 96, 97, 98, or 99 percentidentical to the polypeptide sequence as set forth in SEQ ID NO: 2 (lipBsOspA 1/2²⁵¹), SEQ ID NO: 4 (lipB sOspA 6/4), SEQ ID NO: 6 (lipB sOspA5/3), SEQ ID NO: 8 (sOspA 1/2²⁵¹), SEQ ID NO: 10 (sOspA 6/4), SEQ ID NO:12 (sOspA 5/3), SEQ ID NO: 169 (orig sOspA 1/2), SEQ ID NO: 171 (origsOspA 6/4), or SEQ ID NO: 173 (orig sOspA 5/3).

In some embodiments, methods to determine sequence identity and/orsimilarity are designed to give the largest match between the sequencestested. Methods to determine identity and similarity are described inpublicly available computer programs. In some aspects, computer programmethods to determine identity and similarity between two sequencesinclude, but are not limited to, the GCG program package, including GAP(Devereux et al., Nucl. Acid. Res., 12:387 (1984); Genetics ComputerGroup, University of Wisconsin, Madison, Wis., BLASTP, BLASTN, and FASTA(Altschul et al., J. Mol. Biol., 215:403-410 (1990)). The BLASTX programis publicly available from the National Center for BiotechnologyInformation (NCBI) and other sources (BLAST Manual, Altschul et al.NCB/NLM/NIH Bethesda, Md. 20894; Altschul et al., supra (1990)). Thewell-known Smith Waterman algorithm is also used to determine identity.

Certain alignment schemes for aligning two amino acid sequences, in someaspects, result in the matching of only a short region of the twosequences, and this small aligned region may have very high sequenceidentity even though there is no significant relationship between thetwo full-length sequences. Accordingly, in one embodiment the selectedalignment method (GAP program) will result in an alignment that spans atleast 50 contiguous amino acids of the target polypeptide. For example,using the computer algorithm GAP (Genetics Computer Group, University ofWisconsin, Madison, Wis.), two polypeptides for which the percentsequence identity is to be determined are aligned for optimal matchingof their respective amino acids (the “matched span”, as determined bythe algorithm). A gap opening penalty (which is calculated as 3× theaverage diagonal; the “average diagonal” is the average of the diagonalof the comparison matrix being used; the “diagonal” is the score ornumber assigned to each perfect amino acid match by the particularcomparison matrix) and a gap extension penalty (which is usually 1/10times the gap opening penalty), as well as a comparison matrix such asPAM 250 or BLOSUM 62 are used in conjunction with the algorithm. Astandard comparison matrix (see Dayhoff et al., Atlas of ProteinSequence and Structure, 5(3)(1978) for the PAM 250 comparison matrix;Henikoff et al., Proc. Natl. Acad. Sci. USA, 89:10915-10919 (1992) forthe BLOSUM 62 comparison matrix) is also used by the algorithm.

In various aspects, parameters for a polypeptide sequence comparisoninclude the following:

Algorithm: Needleman et al., J. Mol. Biol., 48:443-453 (1970);

Comparison matrix: BLOSUM 62 from Henikoff et al., supra (1992);

Gap Penalty: 12

Gap Length Penalty: 4

Threshold of Similarity: 0

The GAP program is useful with the above parameters. The aforementionedparameters are the default parameters for polypeptide comparisons (alongwith no penalty for end gaps) using the GAP algorithm.

In some aspects, parameters for nucleic acid molecule sequencecomparisons include the following:

Algorithm: Needleman et al., supra (1970);

Comparison matrix: matches=+10, mismatch=0

Gap Penalty: 50

Gap Length Penalty: 3

The GAP program is also useful with the above parameters. Theaforementioned parameters are the default parameters for nucleic acidmolecule comparisons. Other exemplary algorithms, gap opening penalties,gap extension penalties, comparison matrices, thresholds of similarity,and the like, are used by those of skill in the art, including those setforth in the Program Manual, Wisconsin Package, Version 9, September,1997. The particular choices to be made will be apparent to those ofskill in the art and will depend on the specific comparison to be made,such as DNA-to-DNA, protein-to-protein, protein-to-DNA; andadditionally, whether the comparison is between given pairs of sequences(in which case GAP or BestFit are generally preferred) or between onesequence and a large database of sequences (in which case FASTA orBLASTA are preferred).

Differences in the nucleic acid sequence, in some aspects, result inconservative and/or non-conservative modifications of the amino acidsequence relative to the amino acid sequence of SEQ ID NO: 2 (lipB sOspA1/2²⁵¹), SEQ ID NO: 4 (lipB sOspA 6/4), SEQ ID NO: 6 (lipB sOspA 5/3),SEQ ID NO: 8 (sOspA 1/2²⁵¹), SEQ ID NO: 10 (sOspA 6/4), SEQ ID NO: 12(sOspA 5/3), SEQ ID NO: 169 (orig sOspA 1/2), SEQ ID NO: 171 (orig sOspA6/4), or SEQ ID NO: 173 (orig sOspA 5/3).

Conservative modifications to the amino acid sequence of SEQ ID NO: 2(lipB sOspA 1/2²⁵¹), SEQ ID NO: 4 (lipB sOspA 6/4), SEQ ID NO: 6 (lipBsOspA 5/3), SEQ ID NO: 8 (sOspA 1/2²⁵¹), SEQ ID NO: 10 (sOspA 6/4), SEQID NO: 12 (sOspA 5/3), SEQ ID NO: 169 (orig sOspA 1/2), SEQ ID NO: 171(orig sOspA 6/4), or SEQ ID NO: 173 (orig sOspA 5/3) (and correspondingmodifications to the encoding nucleotides) will produce OspApolypeptides having functional and chemical characteristics similar tothose of a naturally occurring OspA polypeptide. In contrast,substantial modifications in the functional and/or chemicalcharacteristics of OspA polypeptides are accomplished by selectingsubstitutions in the amino acid sequence of SEQ ID NO: 2 (lipB sOspA1/2²⁵¹), SEQ ID NO: 4 (lipB sOspA 6/4), SEQ ID NO: 6 (lipB sOspA 5/3),SEQ ID NO: 8 (sOspA 1/2²⁵¹), SEQ ID NO: 10 (sOspA 6/4), SEQ ID NO: 12(sOspA 5/3), SEQ ID NO: 169 (orig sOspA 1/2), SEQ ID NO: 171 (orig sOspA6/4), or SEQ ID NO: 173 (orig sOspA 5/3) that differ significantly intheir effect on maintaining (a) the structure of the molecular backbonein the area of the substitution, for example, as a sheet or helicalconformation, (b) the charge or hydrophobicity of the molecule at thetarget site, or (c) the bulk of the side chain.

For example, a “conservative amino acid substitution,” in some aspects,involves a substitution of a native amino acid residue with a normativeresidue such that there is little or no effect on the polarity or chargeof the amino acid residue at that position. Furthermore, any nativeresidue in the polypeptide, in certain aspects, is also substituted withalanine, as has been previously described for “alanine scanningmutagenesis.”

Conservative amino acid substitutions also encompass non-naturallyoccurring amino acid residues which are typically incorporated bychemical peptide synthesis rather than by synthesis in biologicalsystems. These include peptidomimetics and other reversed or invertedforms of amino acid moieties.

Naturally occurring residues, in various aspects, are divided intoclasses based on common side chain properties:

1) hydrophobic: norleucine, Met, Ala, Val, Leu, Ile;2) neutral hydrophilic: Cys, Ser, Thr, Asn, Gln;3) acidic: Asp, Glu;4) basic: H is, Lys, Arg;5) residues that influence chain orientation: Gly, Pro; and6) aromatic: Trp, Tyr, Phe.

For example, non-conservative substitutions, in some aspects, involvethe exchange of a member of one of these classes for a member fromanother class. Such substituted residues, in various aspects, areintroduced into regions of the OspA polypeptide that are homologous, orsimilar, with OspA polypeptide orthologs, or into the non-homologousregions of the molecule.

In making such changes, the hydropathic index of amino acids is oftenconsidered. Each amino acid has been assigned a hydropathic index on thebasis of its hydrophobicity and charge characteristics. They are:isoleucine (+4.5); valine (+4.2); leucine (+3.8); phenylalanine (+2.8);cysteine/cystine (+2.5); methionine (+1.9); alanine (+1.8); glycine(−0.4); threonine (−0.7); serine (−0.8); tryptophan (−0.9); tyrosine(−1.3); proline (−1.6); histidine (−3.2); glutamate (−3.5); glutamine(−3.5); aspartate (−3.5); asparagine (−3.5); lysine (−3.9); and arginine(−4.5).

The importance of the hydropathic amino acid index in conferringinteractive biological function on a protein is understood in the art.Kyte et al., J. Mol. Biol., 157:105-131 (1982). It is known that certainamino acids may be substituted for other amino acids having a similarhydropathic index or score and still retain a similar biologicalactivity. In making changes based upon the hydropathic index, thesubstitution of amino acids whose hydropathic indices are within ±2 is,in certain aspects, preferred, those which are within ±1 are, in otheraspects, particularly preferred, and those within ±0.5 are, in variousaspects, more particularly preferred.

It is also understood in the art that the substitution of like aminoacids can be made effectively on the basis of hydrophilicity,particularly where the biologically functional equivalent protein orpeptide thereby created is intended, in part, for use in immunologicalembodiments, as in the present case. The greatest local averagehydrophilicity of a protein, as governed by the hydrophilicity of itsadjacent amino acids, correlates with its immunogenicity andantigenicity, i.e., with a biological property of the protein.

The following hydrophilicity values have been assigned to these aminoacid residues: arginine (+3.0); lysine (+3.0); aspartate (+3.0±1);glutamate (+3.0±1); serine (+0.3); asparagine (+0.2); glutamine (+0.2);glycine (0); threonine (−0.4); proline (−0.5±1); alanine (−0.5);histidine (−0.5); cysteine (−1.0); methionine (−1.3); valine (−1.5);leucine (−1.8); isoleucine (−1.8); tyrosine (−2.3); phenylalanine (−2.5)and tryptophan (−3.4). In making changes based upon similarhydrophilicity values, the substitution of amino acids whosehydrophilicity values are within ±2 is, in certain aspects, preferred,those which are within ±1 are in other aspects, particularly preferred,and those within ±0.5 are, in various aspects, more particularlypreferred. One of skill also identifies epitopes from primary amino acidsequences on the basis of hydrophilicity. These regions are alsoreferred to as “epitopic core regions.”

Desired amino acid substitutions (whether conservative ornon-conservative) can be determined by those skilled in the art at thetime such substitutions are desired. For example, amino acidsubstitutions can be used to identify important residues of the OspApolypeptide, or to increase or decrease the affinity of the OspApolypeptides for their substrates, described herein.

In some aspects, substitutions of nucleotides in nucleotide sequencesand amino acids in amino acid sequences are included in the invention.The substitutions include one to 5, one to 10, one to 15, one to 20, oneto 25, one to 30, one to 35, one to 40, one to 45, one to 50, one to 55,one to 60, one to 65, one to 70, one to 75, one to 80, one to 85, one to90, one to 95, one to 100, one to 150, and one to 200 nucleotides.Likewise, substitutions include one to 5, one to 10, one to 15, one to20, one to 25, one to 30, one to 35, one to 40, one to 45, one to 50,one to 55, one to 60, one to 65, one to 70, one to 75, one to 80, one to85, one to 90, one to 95, and one to 100 amino acids. The substitutions,in various aspects, are conservative or non-conservative.

Exemplary Amino Acid Substitutions are Set Forth in Table 2.

TABLE 2 Amino Acid Substitutions Exemplary Preferred Original ResiduesSubstitutions Substitutions Ala Val, Leu, Ile Val Arg Lys, Gln, Asn LysAsn Gln Gln Asp Glu Glu Cys Ser, Ala Ser Gln Asn Asn Glu Asp Asp GlyPro, Ala Ala His Asn, Gln, Lys, Arg Arg Ile Leu, Val, Met, Ala, Leu Phe,Norleucine Leu Norleucine, Ile, Ile Val, Met, Ala, Phe Lys Arg, 1,4Diamino-butyric Arg Acid, Gln, Asn Met Leu, Phe, Ile Leu Phe Leu, Val,Ile, Ala, Leu Tyr Pro Ala Gly Ser Thr, Ala, Cys Thr Thr Ser Ser Trp Tyr,Phe Tyr Tyr Trp, Phe, Thr, Ser Phe Val Ile, Met, Leu, Phe, Leu Ala,Norleucine

A skilled artisan can determine suitable analogs or variants of thepolypeptide as set forth in SEQ ID NO: 2, 4, 6, 8, 10, 12, 169, 171, or173 using well-known techniques. For identifying suitable areas of themolecule that may be changed without destroying activity, one skilled inthe art may target areas not believed to be important for activity. Forexample, when similar polypeptides with similar activities from the samespecies or from other species are known, one skilled in the art maycompare the amino acid sequence of an OspA polypeptide to such similarpolypeptides. With such a comparison, one can identify residues andportions of the molecules that are conserved among similar polypeptides.It will be appreciated that changes in areas of an OspA polypeptide thatare not conserved relative to such similar polypeptides would be lesslikely to adversely affect the biological activity and/or structure ofthe OspA polypeptide. One skilled in the art would also know that, evenin relatively conserved regions, one may substitute chemically similaramino acids for the naturally occurring residues while retainingactivity (conservative amino acid residue substitutions).

In some embodiments, OspA polypeptide variants include glycosylationvariants wherein the number and/or type of glycosylation sites has beenaltered compared to the amino acid sequence set forth in SEQ ID NO: 2,4, 6, 8, 10, 12, 169, 171, or 173. In one embodiment, OspA polypeptidevariants comprise a greater or a lesser number of N-linked glycosylationsites than the amino acid sequence set forth in SEQ ID NO: 2, 4, 6, 8,10, 12, 169, 171, or 173. An N-linked glycosylation site ischaracterized by the sequence: Asn-X-Ser or Asn-X-Thr, wherein the aminoacid residue designated as X may be any amino acid residue exceptproline. The substitution of amino acid residues to create this sequenceprovides a potential new site for the addition of an N-linkedcarbohydrate chain. Alternatively, substitutions which eliminate thissequence will remove an existing N-linked carbohydrate chain. Alsoprovided is a rearrangement of N-linked carbohydrate chains wherein oneor more N-linked glycosylation sites (typically those that are naturallyoccurring) are eliminated and one or more new N-linked sites arecreated. Additional OspA variants include cysteine variants wherein oneor more cysteine residues are deleted from or substituted for anotheramino acid (e.g., serine) as compared to the amino acid sequence setforth in SEQ ID NO: 2, 4, 6, 8, 10, 12, 169, 171, or 173. Cysteinevariants are useful when OspA polypeptides must be refolded into abiologically active conformation such as after the isolation ofinsoluble inclusion bodies. Cysteine variants generally have fewercysteine residues than the native protein, and typically have an evennumber to minimize interactions resulting from unpaired cysteines.

The invention further provides polypeptides that comprise anepitope-bearing portion of a protein as shown in SEQ ID NO: 2, 4, 6, 8,10, 12, 169, 171, or 173. The term, “epitope” refers to a region of aprotein to which an antibody can bind. See e.g., Geysen et al., Proc.Natl. Acad. Sci. USA 81:3998-4002 (1984). Epitopes can be linear orconformational, the latter being composed of discontinuous regions ofthe protein that form an epitope upon folding of the protein. Linearepitopes are generally at least 6 amino acid residues in length.Relatively short synthetic peptides that mimic part of a proteinsequence are routinely capable of eliciting an antiserum that reactswith the partially mimicked protein. See, Sutcliffe et al., Science219:660-666 (1983). Antibodies that recognize short, linear epitopes areparticularly useful in analytic and diagnostic applications that employdenatured protein, such as Western blotting. See Tobin, Proc. Natl.Acad. Sci. USA, 76:4350-4356 (1979). Antibodies to short peptides, incertain instances, also recognize proteins in native conformation andwill thus be useful for monitoring protein expression and proteinisolation, and in detecting OspA proteins in solution, such as by ELISAor in immunoprecipitation studies.

Synthesis of Chimeric OspA Nucleic Acid Molecules and PolypeptideMolecules

The nucleic acid molecules encode a polypeptide comprising the aminoacid sequence of an OspA polypeptide and can readily be obtained in avariety of ways including, without limitation, recombinant DNA methodsand chemical synthesis.

Recombinant DNA methods are generally those set forth in Sambrook etal., Molecular Cloning: A Laboratory Manual, Cold Spring HarborLaboratory Press, Cold Spring Harbor, N.Y. (1989), and/or Ausubel etal., eds., Current Protocols in Molecular Biology, Green Publishers Inc.and Wiley and Sons, NY (1994). Recombinant expression techniquesconducted in accordance with the descriptions set forth below, invarious aspects, are followed to produce these polynucleotides and toexpress the encoded polypeptides. For example, by inserting a nucleicacid sequence which encodes the amino acid sequence of an OspApolypeptide into an appropriate vector, one skilled in the art canreadily produce large quantities of the desired nucleotide sequence. Thesequences can then be used to generate detection probes or amplificationprimers. Alternatively, a polynucleotide encoding the amino acidsequence of an OspA polypeptide can be inserted into an expressionvector. By introducing the expression vector into an appropriate host,the encoded OspA polypeptide or OspA polypeptides are, in some aspects,produced in large amounts.

Likewise, chemical synthesis of nucleic acids and polypeptides are wellknown in the art, such as those described by Engels et al., Angew. Chem.Intl. Ed., 28:716-734 (1989). These methods include, inter alia, thephosphotriester, phosphoramidite and H-phosphonate methods for nucleicacid synthesis. In one aspect, a method for such chemical synthesis ispolymer-supported synthesis using standard phosphoramidite chemistry.Typically, the DNA encoding the amino acid sequence of an OspApolypeptide will be several hundred nucleotides in length. Nucleic acidslarger than about 100 nucleotides are synthesized as several fragmentsusing these methods. The fragments are then ligated together to form thefull-length nucleotide sequences of the invention. In particularaspects, the DNA fragment encoding the amino terminus of the polypeptidehas an ATG, which encodes a methionine residue.

In a particular aspect of the invention, chimeric OspA coding sequencesare made using synthetic overlapping oligonucleotides. Because DNA fromBorrelia cells is not used, a further benefit of the synthetic approachis the avoidance of contamination with adventitious agents contained inmaterial of animal origin (i.e. serum or serum albumin) present inBorrelia culture medium. This strategy also substantially reduces thenumber of manipulations required to make the chimeric genes, since itallows sequence alterations to be made in a single step, such asmodifications to optimize expression (OspB leader sequence), tointroduce restriction sites to facilitate cloning, or to avoid potentialintellectual property issues. It also enables codon usage to beoptimized for an E. coli host, since the presence of codons that arerarely used in E. coli is known to present a potential impediment tohigh-level expression of foreign genes (Makoff et al., Nucleic AcidsRes. 17:10191-202, 1989; Lakey et al., Infect. Immun. 68:233-8, 2000).Other methods known to the skilled artisan are used as well.

In certain embodiments, nucleic acid variants contain codons which havebeen altered for the optimal expression of an OspA polypeptide in agiven host cell. Particular codon alterations depend upon the OspApolypeptide(s) and host cell(s) selected for expression. Such “codonoptimization” can be carried out by a variety of methods, for example,by selecting codons which are preferred for use in highly expressedgenes in a given host cell. Computer algorithms which incorporate codonfrequency tables such as “Ecohigh.cod” for codon preference of highlyexpressed bacterial genes are used, in some instances, and are providedby the University of Wisconsin Package Version 9.0, Genetics ComputerGroup, Madison, Wis. Other useful codon frequency tables include“Celegans_high.cod”, “Celegans_low.cod”, “Drosophila_high.cod”,“Human_high.cod”, “Maize_high.cod”, and “Yeast_high.cod.”

A nucleic acid molecule encoding the amino acid sequence of an OspApolypeptide, in certain aspects, is inserted into an appropriateexpression vector using standard ligation techniques. The vector istypically selected to be functional in the particular host cell employed(i.e., the vector is compatible with the host cell machinery such thatamplification of the gene and/or expression of the gene can occur). Anucleic acid molecule encoding the amino acid sequence of an OspApolypeptide, in various aspects, is amplified/expressed in prokaryotic,yeast, insect (baculovirus systems), and/or eukaryotic host cells.Selection of the host cell depends in part on whether an OspApolypeptide is to be post-translationally modified (e.g., glycosylatedand/or phosphorylated). If so, yeast, insect, or mammalian host cellsare preferable. For a review of expression vectors, see Meth. Enz., vol.185, D. V. Goeddel, ed., Academic Press Inc., San Diego, Calif. (1990).

Cloning vectors include all those known in the art. See, e.g., Sambrook,Fritsch & Maniatis, Molecular Cloning: A Laboratory Manual, SecondEdition. Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory Press,1989. In one aspect, pUC18 is used as the cloning vector for allintermediate steps, because genetic manipulations and sequencing areeasier with this plasmid than with the vector pET30a. The principalfeatures are notably, the lacZ gene fragment coding for LacZ alphapeptide from base pairs 149 to 469 (lac promoter at base pairs 507), thebla gene encoding the ampicillin resistance determinant from base pairs1629 to 2486 (bla promoter at base pairs 2521), the origin ofreplication at base pairs 867 and multiple cloning sites from base pairs185 to 451 (FIG. 12).

Expression vectors include all those known in the art, including withoutlimitation cosmids, plasmids (e.g., naked or contained in liposomes) andviruses that incorporate the recombinant polynucleotide. The expressionvector is inserted (e.g., via transformation or transduction) into anappropriate host cell for expression of the polynucleotide andpolypeptide via transformation or transfection using techniques known inthe art. See, e.g., Sambrook, Fritsch & Maniatis, Molecular Cloning: ALaboratory Manual, Second Edition. Cold Spring Harbor, N.Y.: Cold SpringHarbor Laboratory Press, 1989. In one aspect, pET30a (Novagen) is usedas the expression vector for the final complete OspA gene insert. In pETvectors, genes are cloned under the control of a T7 promoter andexpression is induced by providing a source of T7 RNA polymerase in thehost cell (no expression occurs until a source of T7 RNA polymerase isprovided). The principal features are the gene encoding kanamycinresistance (kan) at base pairs 4048 to 4860, the lacI gene base pairs826-1905, the F1 origin of replication at base pairs 4956-5411 andmultiple cloning sites from base pairs 158 to 346 (FIG. 13).

After the vector has been constructed and a nucleic acid moleculeencoding an OspA polypeptide has been inserted into the proper site ofthe vector, the completed vector is inserted into a suitable host cellfor amplification and/or polypeptide expression. The transformation ofan expression vector for an OspA polypeptide into a selected host cellis, in various aspects, accomplished by well-known methods such astransfection, infection, calcium chloride-mediated transformation,electroporation, microinjection, lipofection or the DEAE-dextran methodor other known techniques. The method selected will in part be afunction of the type of host cell to be used. These methods and othersuitable methods are well known to the skilled artisan and are setforth, for example, in Sambrook et al., supra.

Host cells, in some aspects, are prokaryotic host cells (such as E.coli) or eukaryotic host cells (such as yeast, insect or vertebratecells). The host cell, when cultured under appropriate conditions,synthesizes an OspA polypeptide which can subsequently be collected fromthe culture medium (if the host cell secretes it into the medium) ordirectly from the host cell producing it (if it is not secreted). Theselection of an appropriate host cell depends upon various factors, suchas desired expression levels, polypeptide modifications that aredesirable or necessary for activity (such as glycosylation orphosphorylation), and ease of folding into a biologically activemolecule. Such host cells include, but are not limited to, host cells ofbacterial, yeast, fungal, viral, invertebrate, and mammalian sources.For examples of such host cells, see Maniatis et al., Molecular Cloning:A Laboratory Manual, Cold Spring Harbor Laboratory, Cold Spring Harbor,N.Y. (1989). In additional aspects, host cells used in the art since thepublication of the Maniatis (supra) manual are also used in theinvention.

In one aspect, the host cell is an E. coli cell. Suitable strains of E.coli include, but are not limited to, BL21, DH5α, HMS174(DE3), DH10B, orE. CLONI 10G (Lucigen, Middleton, Wis.). In some embodiments, host cellsare engineered to enhance transformation efficiency and/or maintenanceof the vector.

In one aspect, the E. coli strain DH5α [genotype: end A1 hsdR17 (rK-mK+)supE44 thi-1 recA1 gyrA (Nalr) relA1 D(lacZYA-argF)U169 deoR(F80dlacD(lacZ)M15] (Gibco BRL) is used for all intermediate cloningsteps. This strain is derived from E. coli strain K12, one of the mostwidely used hosts in genetic engineering. The strain is amp- to allowselection of transformants with vectors containing the ampicillinresistance gene (amp).

In another aspect, the E. coli strain HMS174(DE3) is used as the hostfor expression. E. coli HMS174(DE3) host cells [genotype: F-recA1 hsdR(rk12-mk12+) RifR (DE3)] (Novagen) are used in various examplesdescribed herein for the final cloning steps. The strain is kan- toallow selection of transformants with vectors containing the kanamycinresistance gene (kan).

Host cells comprising an OspA polypeptide expression vector are culturedusing standard media well known to the skilled artisan. The media willusually contain all nutrients necessary for the growth and survival ofthe cells. Suitable media for culturing E. coli cells include, forexample, Luria Broth (LB) and/or Terrific Broth (TB). Suitable media forculturing eukaryotic cells include Roswell Park Memorial Institutemedium 1640 (RPMI 1640), Minimal Essential Medium (MEM) and/orDulbecco's Modified Eagle Medium (DMEM), all of which, in someinstances, are supplemented with serum and/or growth factors asindicated by the particular cell line being cultured. A suitable mediumfor insect cultures is Grace's medium supplemented with yeastolate,lactalbumin hydrolysate and/or fetal calf serum, as necessary.

Typically, an antibiotic or other compound useful for selective growthof transformed cells is added as a supplement to the media. The compoundto be used will be dictated by the selectable marker element present onthe plasmid with which the host cell was transformed. For example, wherethe selectable marker element is kanamycin resistance, the compoundadded to the culture medium will be kanamycin. Other compounds forselective growth include ampicillin, tetracycline and neomycin.

The amount of an OspA polypeptide produced by a host cell can beevaluated using standard methods known in the art. Such methods include,without limitation, Western blot analysis, SDS-polyacrylamide gelelectrophoresis, non-denaturing gel electrophoresis, chromatographicseparation such as High Performance Liquid Chromatography (HPLC),immunodetection such as immunoprecipitation, and/or activity assays suchas DNA binding gel shift assays.

In some cases, an OspA polypeptide is not biologically active uponisolation. Various methods for “refolding” or converting the polypeptideto its tertiary structure and generating disulfide linkages are used torestore biological activity. Such methods include exposing thesolubilized polypeptide to a pH usually above 7 and in the presence of aparticular concentration of a chaotrope. The selection of chaotrope isvery similar to the choices used for inclusion body solubilization, butusually the chaotrope is used at a lower concentration and is notnecessarily the same as chaotropes used for the solubilization. In someinstances, the refolding/oxidation solution also contains a reducingagent or the reducing agent plus its oxidized form in a specific ratioto generate a particular redox potential allowing for disulfideshuffling to occur in the formation of the protein's cysteine bridge(s).Some of the commonly used redox couples include cysteine/cystamine,glutathione (GSH)/dithiobis GSH, cuprous chloride, dithiothreitol(DTT)/dithiane DTT, and 2-2mercaptoethanol (bME)/dithio-b (ME). Acosolvent is often used to increase the efficiency of the refolding, andthe more common reagents used for this purpose include glycerol,polyethylene glycol of various molecular weights, arginine and the like.

If inclusion bodies are not formed to a significant degree uponexpression of an OspA polypeptide, then the polypeptide will be foundprimarily in the supernatant after centrifugation of the cellhomogenate. The polypeptide is further isolated from the supernatantusing methods such as those described herein or otherwise known in theart.

The purification of an OspA polypeptide from solution can beaccomplished using a variety of techniques known in the art. If thepolypeptide has been synthesized such that it contains a tag such asHexahistidine (OspA polypeptide/hexaHis) or other small peptide such asFLAG (Eastman Kodak Co., New Haven, Conn.) or myc (Invitrogen, Carlsbad,Calif.) at either its carboxyl or amino terminus, the polypeptide isoften purified in a one-step process by passing the solution through anaffinity column where the column matrix has a high affinity for the tag.For example, polyhistidine binds with great affinity and specificity tonickel; thus an affinity column of nickel (such as the Qiagen® nickelcolumns) can be used for purification of OspA polypeptide/polyHis. Seefor example, Ausubel et al., eds., Current Protocols in MolecularBiology, Section 10.11.8, John Wiley & Sons, New York (1993).

Additionally, the OspA polypeptide may be purified through use of amonoclonal antibody which is capable of specifically recognizing andbinding to the OspA polypeptide. Suitable procedures for purificationthus include, without limitation, affinity chromatography,immunoaffinity chromatography, ion exchange chromatography, molecularsieve chromatography, High Performance Liquid Chromatography (HPLC),electrophoresis (including native gel electrophoresis) followed by gelelution, and preparative isoelectric focusing (“Isoprime”machine/technique, Hoefer Scientific, San Francisco, Calif.). In somecases, two or more purification techniques are combined to achieveincreased purity.

OspA polypeptides are also prepared by chemical synthesis methods (suchas solid phase peptide synthesis) using techniques known in the art,such as those set forth by Merrifield et al., J. Am. Chem. Soc., 85:2149(1963), Houghten et al., Proc. Natl. Acad. Sci. USA, 82:5132 (1985), andStewart and Young, “Solid Phase Peptide Synthesis”, Pierce Chemical Co.,Rockford, Ill. (1984). Such polypeptides are synthesized with or withouta methionine on the amino terminus. Chemically synthesized OspApolypeptides, in some aspects, are oxidized using methods set forth inthese references to form disulfide bridges. Chemically synthesized OspApolypeptides are expected to have comparable biological activity to thecorresponding OspA polypeptides produced recombinantly or purified fromnatural sources, and thus are often used interchangeably with arecombinant OspA polypeptide. It is appreciated that a number ofadditional methods for producing nucleic acids and polypeptides areknown in the art, and the methods can be used to produce OspApolypeptides.

Chemical Derivatives of OspA Polypeptide Molecules

Chemically modified derivatives of the OspA polypeptides are prepared byone skilled in the art, given the disclosures set forth herein below.OspA polypeptide derivatives are modified in a manner that is differenteither in the type or location of the molecules naturally attached tothe polypeptide. Derivatives, in some aspects, include molecules formedby the deletion of one or more naturally-attached chemical groups. Thepolypeptide comprising the amino acid sequence of SEQ ID NO: 2, 4, 6, 8,10, 12, 169, 171, or 173, or an OspA polypeptide variant, in one aspect,is modified by the covalent attachment of one or more polymers. Forexample, the polymer selected is typically water soluble so that theprotein to which it is attached does not precipitate in an aqueousenvironment, such as a physiological environment. Included within thescope of suitable polymers is a mixture of polymers. In certain aspects,for therapeutic use of the end-product preparation, the polymer will bepharmaceutically acceptable.

The polymers each are, in various aspects, of any molecular weight andare branched or unbranched. The polymers each typically have an averagemolecular weight of between about 2 kDa to about 100 kDa (the term“about” indicating that in preparations of a water-soluble polymer, somemolecules will weigh more, some less, than the stated molecular weight).The average molecular weight of each polymer is, in various aspects,between about 5 kDa to about 50 kDa, between about 12 kDa to about 40kDa, and between about 20 kDa to about 35 kDa.

Suitable water-soluble polymers or mixtures thereof include, but are notlimited to, N-linked or O-linked carbohydrates; sugars; phosphates;polyethylene glycol (PEG) (including the forms of PEG that have beenused to derivatize proteins, including mono-(C1-C10) alkoxy- oraryloxy-polyethylene glycol); monomethoxy-polyethylene glycol; dextran(such as low molecular weight dextran of, for example, about 6 kDa);cellulose; or other carbohydrate-based polymers, poly-(N-vinylpyrrolidone)polyethylene glycol, propylene glycol homopolymers, apolypropylene oxide/ethylene oxide co-polymer, polyoxyethylated polyols(e.g., glycerol) and polyvinyl alcohol. Also encompassed by the presentinvention are bifunctional crosslinking molecules which are sometimesused to prepare covalently attached multimers of the polypeptidecomprising the amino acid sequence of SEQ ID NO: 2, 4, 6, 8, 10, 12,169, 171, or 173, or an OspA polypeptide variant.

In some aspects, chemical derivatization is performed under any suitablecondition used to react a protein with an activated polymer molecule.Methods for preparing chemical derivatives of polypeptides generallycomprise the steps of (a) reacting the polypeptide with the activatedpolymer molecule (such as a reactive ester or aldehyde derivative of thepolymer molecule) under conditions whereby the polypeptide comprisingthe amino acid sequence of SEQ ID NO: 2, 4, 6, 8, 10, 12, 169, 171, or173, or an OspA polypeptide variant becomes attached to one or morepolymer molecules, and (b) obtaining the reaction product(s). Theoptimal reaction conditions are determined based on known parameters andthe desired result. For example, the larger the ratio of polymermolecules:protein, the greater the percentage of attached polymermolecule. In one embodiment, the OspA polypeptide derivative has asingle polymer molecule moiety at the amino terminus (see, for example,U.S. Pat. No. 5,234,784).

The pegylation of the polypeptide, in certain aspects, is specificallycarried out by any of the pegylation reactions known in the art, asdescribed for example in the following references: Francis et al., Focuson Growth Factors, 3:4-10 (1992); EP 0154316; EP 0401384 and U.S. Pat.No. 4,179,337. For example, pegylation is carried out via an acylationreaction or an alkylation reaction with a reactive polyethylene glycolmolecule (or an analogous reactive water-soluble polymer) as describedherein. For the acylation reactions, the polymer(s) selected should havea single reactive ester group. For reductive alkylation, the polymer(s)selected should have a single reactive aldehyde group. A reactivealdehyde is, for example, polyethylene glycol propionaldehyde, which iswater stable, or mono C1-C10 alkoxy or aryloxy derivatives thereof (seeU.S. Pat. No. 5,252,714).

In another embodiment, OspA polypeptides are chemically coupled tobiotin, and the biotin/OspA polypeptide molecules which are conjugatedare then allowed to bind to avidin, resulting in tetravalentavidin/biotin/OspA polypeptide molecules. OspA polypeptides are alsocovalently coupled to dinitrophenol (DNP) or trinitrophenol (TNP) andthe resulting conjugates precipitated with anti-DNP or anti-TNP-IgM toform decameric conjugates with a valency of 10. The OspA polypeptidederivatives disclosed herein, in certain aspects, have additionalactivities, enhanced or reduced biological activity, or othercharacteristics, such as increased or decreased half-life, as comparedto the non-derivatized molecules.

Immunogenic Compositions, Vaccines, and Antibodies

Some aspects of the invention include immunogenic compositions andvaccines. Immunogenic chimeric OspA molecules of the invention are usedin combination as antigen(s) to elicit an anti-OspA immune response in asubject (i.e., act as a vaccine). Exemplary immunogenic OspApolypeptides (SEQ ID NOS: 2, 4, 6, 169, 171, and 173) are delivered incombination to elicit an immune response to any one or more of serotypes1-6 of Borrelia, and more generally to many other species of Borrelia asdiscussed herein. An immune response can also be raised by delivery ofplasmid vectors encoding the OspA polypeptides of the invention (i.e.,administration of “naked DNA”). In some aspects, OspA nucleic acidmolecules (SEQ ID NOS: 1, 3, 5, 168, 170, and 172) are delivered byinjection, via liposomes, or by other means of administration describedherein. Once immunized, the subject elicits a heightened immune responseagainst the OspA protein of serotypes 1-6 of Borrelia and against otherspecies of Borrelia.

As set out above, therefore, both OspA polypeptides and OspA nucleicacid molecules are included as antigens for use in the immunogenicand/or vaccine compositions of the invention. In certain aspects, boththe nucleic acid and the protein are delivered to the subject. Inparticular aspects, the immune response to a nucleic acid vaccine isproposed to be enhanced by simultaneous administration of a cognateprotein (see WO 99/30733). The nucleic acid and protein do not need tobe administered in the same composition. Both must merely beadministered during the induction phase of the immune response with theprotein, in some aspects, being masked or held back until after thenucleic acid has primed the immune system. In a particular aspect,vaccines are intended to deliver nucleic acid and protein antigen intoantigen presenting cells (see WO 97/28818). In various aspects, thenucleic acid and protein are complexed, e.g., by covalent conjugation.In further aspects, liposomal formulations are also included to enhancethe immunogenicity of vaccine antigens.

In certain aspects, an immunogenic composition of the invention includesany one or more of the OspA molecules described herein in combinationwith a pharmaceutical carrier, wherein the composition inducesproduction of an antibody that specifically binds an Outer surfaceprotein A (OspA) protein. In some aspects, the immunogenic compositionalso comprises a stabilizer or antimicrobial preservative. In particularaspects, the immunogenic composition induces production of an antibodythat specifically binds Borrelia. In other aspects, the compositioninduces production of an antibody that neutralizes Borrelia.

In some aspects, the invention includes the use of adjuvants in theimmunogenic compositions comprising the chimeric OspA molecules(antigens) described herein. In certain aspects, immunogenicity issignificantly improved if an antigen is co-administered with anadjuvant. In some aspects, an adjuvant is used as 0.001% to 50% solutionin phosphate buffered saline (PBS). Adjuvants enhance the immunogenicityof an antigen but are not necessarily immunogenic themselves.

Adjuvants, in various aspects, have a number of positive effects onvaccination. In some instances, adjuvants accelerate the generation of arobust immune response in subjects. Adjuvants, in other instances,increase the level of immune response, prolong its duration and improveimmune memory. Adjuvants are often used to overcome weakened immunity ofparticular subject groups (e.g., the elderly or immune-suppressedpatients) or to improve the immunogenicity of particular “at risk group”(such as, but not limited to, the very young or elderly). The immuneenhancing effects of an adjuvant, in various instances, leads to areduction of the amount of antigen required in the final formulation togive a protective response (i.e. dose-sparing).

In general, adjuvants are classified, based on their dominant mechanismof action, into two main groups: The first group are the agonists ofinnate immunity system receptors or sensors, such as Toll-like-receptor(TLR) agonists, C-type lectin receptor agonists, retinoic acid induciblegene 1 (RIG-1) like receptor (RLR) agonists, and nucleotide-bindingdomain and leucine rich repeat-containing receptor (NLR) agonists. Thesecond group are the substances which act as delivery systems, alsoknown as TLR-independent adjuvants. Examples of TLR agonist adjuvantsare ASO4 (Glaxo Smith Kline), a TLR-4 agonist, used as an adjuvant incommercial Hepatitis B and papillioma virus vaccines; Vaxinate, aflagellin-fusion protein TLR-5 agonist; and numerous TLR-9 agonistadjuvants, such as those that use double-stranded DNA (dsDNA) andoligonucleotides CpG or ODN1a. Other TLR-agonists falling into thiscategory of adjuvants include glycolipids (TLR-1), lipoteichoic acid andlipoprotein (TLR-1/TLR-2 and TLR-2/TLR-6) lipopolysaccharide,lipooligocaccharides and monophosphoryt lipid A (MPL) (TLR-4),double-stranded RNA (TLR-3); peptidoglycan (TLR-6), single stranded RNA(TLR-7). Examples of two C-type lectin receptor agonist adjuvantsinclude β-glucans (Dectin-1) and mannans (Dectin-2), both derived fromfungal cell walls. RLR receptor agonist adjuvants includesingle-stranded viral RNA and double-stranded viral DNA, while NLRagonist adjuvants include peptidoglycan degradation products, microbialproducts, and non-infectious crystal particles. In all cases, theagonists act by directly activating the innate immune system receptor totrigger an immune enhancing inflammatory response. The second group ofadjuvants, the TLR independent adjuvants, mostly act as delivery systemsand enhance antigen uptake and presentation by an antigen presentingcell. In some instances, these adjuvants can also act by retaining theantigen locally near the site of administration to produce a depoteffect facilitating a slow, sustained release of antigen to cells of theimmune system. Adjuvants also attract cells of the immune system to anantigen depot and stimulate such cells to elicit immune responses.Examples of TLR independent adjuvants include mineral salts, such asaluminum hydroxide and aluminum phosphate (collectively referred to asalum) and calcium phosphate; oil-in-water emulsion (e.g., MF59, AS03 andProVax); water in oil emulsion (Montanide, TiterMax); biopolymers(Advax); plant derivatives, especially fractions of saponin, atriterpenoid extract from the bark of the South American Molina soaptree Quillaja saponaria (SFA-1, QS21, Quil A); immune stimulatingcomplexes (ISCOM and ISCOM matrix) composed of saponin fractions, steroland, optionally, phospholipids (ISCOMATRIX and Matrix-M); liposomes,which are phospholipid spheres of various sizes and charge (Vaxfectinand Vaxisome); virus-like particles and virosomes, which are liposomescontaining viral surface antigens, such as Influenza haemagglutinin andneuraminidase; nanoparticles of various composition; chitosan, peptidessuch as polyarginine and a peptide known as the KLK peptide.

The adjuvants listed herein above are used singly or in combination.Combinations of TLR-dependent and a TLK-independent adjuvants are oftenpreferred as the antigen and the TLR-dependent adjuvant are believed tobe trafficked to antigen presenting cells by the TLR-independentadjuvant, which would also stimulate uptake and stability, while theTLR-dependent adjuvant would directly enhance immunity through theactivation of TLR signaling.

Examples of TLR-dependent and TLR-independent adjuvant combinationsinclude AS01: a mixture of MPL (a TLR-4 agonist), liposomes and QS-21(both TLR-independent adjuvant); AS04: MPL (a TLR-4 agonist) andaluminum hydroxide/phosphate; IC31: ODN1a (a TLR-9 agonist) and KLKpeptide (a TLR-independent adjuvant); and Freunds complete adjuvant, amembrane extract of Mycobacterium tuberculosis (TLR-4 agonist) and aoil-in-water emulsion (a TLR-independent adjuvant).

Combinations consisting of multiple TLR-dependent adjuvants are alsoused to maximize the immune enhancing effect of adjuvanted vaccineformulations. Agonists of TLRs, which use different adaptor proteins,are often combined (e.g., a combination of an agonist for the plasmamembrane-bound TLR-3 or TLR-4 receptor which utilizes the TRIF(Toll/interleukin 1 receptor domain-containing adaptor protein inducingINF-β) adaptor pathway with an agonist of the TLRs (TLR-7, TLR-8 andTLR-9), which are expressed in endosomal or lysosomal organelles andutilize the MyD88 (myeloid differentiating primary response protein)adaptor protein pathway).

These immunostimulatory agents or adjuvants improve the host immuneresponse in vaccines as well. In some cases, substances such aslipopolysaccarides can act as intrinsic adjuvants since they normallyare the components of the killed or attenuated bacteria used asvaccines. Extrinsic adjuvants, such as those listed herein above, areimmunomodulators which are typically non-covalently linked to antigensand are formulated to enhance the host immune response.

A wide range of extrinsic adjuvants can provoke potent immune responsesto antigens. These include saponins complexed to membrane proteinantigens (immune stimulating complexes), pluronic polymers with mineraloil, killed mycobacteria in mineral oil, Freund's complete adjuvant,bacterial products, such as muramyl dipeptide (MDP) andlipopolysaccharide (LPS), as well as lipid A, and liposomes. Toefficiently induce humoral immune response (HIR) and cell-mediatedimmunity (CMI), immunogens are, in certain aspects, emulsified inadjuvants.

Desirable characteristics of ideal adjuvants include any or all of: lackof toxicity; ability to stimulate a long-lasting immune response;simplicity of manufacture and stability in long-term storage; ability toelicit both CMI and HIR to antigens administered by various routes;synergy with other adjuvants; capability of selectively interacting withpopulations of antigen presenting cells (APC); ability to specificallyelicit appropriate T_(H1) or T_(H2) cell-specific immune responses; andability to selectively increase appropriate antibody isotype levels (forexample IgA) against antigens.

U.S. Pat. No. 4,855,283, incorporated herein by reference, theretoteaches glycolipid analogs including N-glycosylamides, N-glycosylureasand N-glycosylcarbamates, each of which is substituted in the sugarresidue by an amino acid, as immune-modulators or adjuvants. U.S. Pat.No. 4,855,283 reported that N-glycolipids analogs displaying structuralsimilarities to the naturally occurring glycolipids, such asglycosphingolipids and glycoglycerolipids, are capable of elicitingstrong immune responses in both herpes simplex virus vaccine andpseudorabies virus vaccine. Some glycolipids have been synthesized fromlong chain alkylamines and fatty acids that are linked directly with thesugar through the anomeric carbon atom, to mimic the functions of thenaturally occurring lipid residues.

In some aspects, the immunogenic composition contains an amount of anadjuvant sufficient to enhance the immune response to the immunogen.Suitable adjuvants include, but are not limited to, aluminium salts(aluminium phosphate or aluminium hydroxide), squalene mixtures (SAF-1),muramyl peptide, saponin derivatives, mycobacterium cell wallpreparations, monophosphoryl lipid A, mycolic acid derivatives,non-ionic block copolymer surfactants, Quil A, cholera toxin B subunit,polphosphazene and derivatives, and immunostimulating complexes (ISCOMs)such as those described by Takahashi et al. (Nature 344:873-875, 1990).In some aspects, the adjuvant is a synthetic adjuvant. In a particularaspect, the synthetic adjuvant is glucopyranosyl lipid adjuvant (GLA).

A further aspect of the invention is a vaccine comprising theimmunogenic composition of the invention and a pharmaceuticallyacceptable carrier. As discussed herein above, the vaccine, in certainaspects, includes one or more stabilizers and/or one or morepreservatives.

In one aspect, there is provided a vaccine comprising at least onerecombinant expression construct which comprises a promoter operablylinked to a nucleic acid sequence encoding an antigen (chimeric OspApolypeptide described herein) and an adjuvant. In one embodiment therecombinant expression construct (expression vector comprising the OspApolynucleotide) is present in a viral vector, which in certain furtherembodiments is present in a virus that is selected from an adenovirus,an adeno-associated virus, a herpesvirus, a lentivirus, a poxvirus, anda retrovirus.

Further aspects of the invention include antibodies to the chimeric OspAmolecules described herein. In various aspects, the invention includesthe chimeric OspA molecules to make anti-OspA antibodies and to provideimmunity from Borrelia infection. In some aspects, these anti-OspAantibodies, e.g., murine, human, or humanized monoclonal antibodies orsingle chain antibodies, are administered to a subject (e.g., passiveimmunization) to effect an immune response against the OspA protein ofany one or more of serotypes 1-6 of Borrelia. As used herein, the term“antibodies” refers to a molecule which has specificity for one or moreOspA polypeptides. Suitable antibodies are prepared using methods knownin the art. In certain aspects, an OspA antibody is capable of binding acertain portion of the OspA polypeptide thereby inhibiting the bindingof the polypeptide to the OspA polypeptide receptor(s). Antibodies andantibody fragments that bind the chimeric OspA polypeptides of theinvention are within the scope of the present invention.

In some aspects, antibodies of the invention include an antibody orfragment thereof that specifically binds one or more OspA polypeptidesproduced by immunizing an animal with a polypeptide comprising the aminoacid sequence selected from the group consisting of SEQ ID NOS: 2, 4, 6,8, 10, 12, 169, 171, and 173. In other aspects, the invention includesan antibody or fragment thereof that specifically binds to a polypeptideencoded by a nucleic acid sequence selected from the group consisting ofSEQ ID NOS: 1, 3, 5, 7, 9, 11, 168, 170, and 172. In various aspects,the antibody or fragment thereof is human, humanized, polyclonal, ormonoclonal. In further aspects, the antibody is an Fab or an Fab′antibody. In particular aspects, the antibody comprises a detectablelabel. In some aspects, the antibody is a chemically modified derivativeof the antibody.

The administration of the chimeric OspA molecules in accordance with theinvention stimulates an immune or antibody response in humans oranimals. In some aspects, three chimeric OspA molecules (e.g., lipidatedOspA 1/2²⁵¹, lipidated OspA 6/4 OspA, and lipidated OspA 5/3; ororiginal OspA 1/2, original OspA 6/4, and original OspA 5/3) areadministered together to elicit antibody response against all sixserotypes (1-6) discussed herein. This antibody response means that theinventive methods are, in various aspects, used for merely stimulatingan immune response (as opposed to also being a protective response)because the resultant antibodies (without protection) are nonethelessuseful. From eliciting antibodies, by techniques well-known in the art,monoclonal antibodies are prepared; and, those monoclonal antibodies areemployed in well known antibody binding assays, diagnostic kits or teststo determine the presence or absence of Borrelia burgdorferi s.l. or todetermine whether an immune response to the spirochete has simply beenstimulated. The monoclonal antibodies, in certain aspects, are employedin immunoadsorption chromatography to recover or isolate Borreliaantigens such as OspA.

The OspA antibodies of the invention, in various aspects, arepolyclonal, including monospecific polyclonal, monoclonal (MAbs),recombinant, chimeric, humanized such as CDR-grafted, human, singlechain, and/or bispecific, as well as fragments, variants or derivativesthereof. Antibody fragments include those portions of the antibody whichbind to an epitope on the OspA polypeptide. Examples of such fragmentsinclude Fab and F(ab′) fragments generated by enzymatic cleavage offull-length antibodies. Other binding fragments include those generatedby recombinant DNA techniques, such as the expression of recombinantplasmids containing nucleic acid sequences encoding antibody variableregions.

Polyclonal antibodies directed toward an OspA polypeptide generally areproduced in a subject (including rabbits, mice, or other animal ormammal) by means of multiple subcutaneous, intramuscular orintraperitoneal injections of OspA polypeptide and an adjuvant. It isuseful, in certain aspects, to conjugate an OspA polypeptide of theinvention to a carrier protein that is immunogenic in the species to beimmunized, such as keyhole limpet hemocyanin, serum, albumin, bovinethyroglobulin, or soybean trypsin inhibitor. Also, adjuvants, such asalum, are used to enhance the immune response. After immunization, bloodsamples are drawn from the subject immunized and the serum is assayedfor anti-OspA polypeptide antibody titer.

Monoclonal antibodies directed toward an OspA polypeptide are producedusing any method which provides for the production of antibody moleculesby continuous cell lines in culture. Examples of suitable methods forpreparing monoclonal antibodies include the hybridoma methods of Kohleret al., Nature, 256:495-497 (1975) and the human B-cell hybridomamethod, Kozbor, J. Immunol., 133:3001 (1984) and Brodeur et al.,Monoclonal Antibody Production Techniques and Applications, pp. 51-63(Marcel Dekker, Inc., New York, 1987). Also provided by the inventionare hybridoma cell lines which produce monoclonal antibodies reactivewith OspA polypeptides.

Monoclonal antibodies of the invention, in some instances, are modifiedfor use as therapeutics. One embodiment is a “chimeric” antibody inwhich a portion of the heavy and/or light chain is identical with orhomologous to a corresponding sequence in antibodies derived from aparticular species or belonging to a particular antibody class orsubclass, while the remainder of the chain(s) is/are identical with orhomologous to a corresponding sequence in antibodies derived fromanother species or belonging to another antibody class or subclass. Alsoincluded are fragments of such antibodies, so long as they exhibit thedesired biological activity. See, U.S. Pat. No. 4,816,567 and Morrisonet al., Proc. Natl. Acad. Sci. USA, 81:6851-6855 (1985).

In another embodiment, a monoclonal antibody of the invention is a“humanized” antibody. Methods for humanizing non-human antibodies arewell known in the art (see U.S. Pat. Nos. 5,585,089, and 5,693,762).Generally, a humanized antibody has one or more amino acid residuesintroduced into it from a source which is non-human. Humanization can beperformed, for example, using methods described in the art (Jones etal., Nature 321:522-525 (1986); Riechmann et al., Nature 332:323-327(1988); Verhoeyen et al., Science 239:1534-1536 (1988)), by substitutingat least a portion of a rodent complementarity-determining region (CDR)for the corresponding regions of a human antibody.

In an alternative embodiment, human antibodies are produced fromphage-display libraries (Hoogenboom et al., J. Mol. Biol. 227:381 (1991)and Marks et al., J. Mol. Biol. 222:581 (1991)). These processes mimicimmune identification through the display of antibody repertoires on thesurface of filamentous bacteriophage, and subsequent selection of phageby their binding to an antigen of choice. One such technique isdescribed in PCT Application No. PCT/US98/17364 (Adams et al.), whichdescribes the isolation of high affinity and functionally agonisticantibodies for MPL- and msk-receptors using such an approach.

Chimeric, CDR grafted, and humanized antibodies are typically producedby recombinant methods. Nucleic acids encoding the antibodies areintroduced into host cells and expressed using materials and proceduresdescribed herein or known in the art. In one embodiment, the antibodiesare produced in mammalian host cells, such as CHO cells. Monoclonal(e.g., human) antibodies are, in various aspects, produced by theexpression of recombinant DNA in host cells or by expression inhybridoma cells as described herein. In some aspects, the monoclonalantibody or fragment thereof is humanized. In a particular aspect, themonoclonal antibody is F237/BK2 as described herein.

In certain aspects, the invention includes methods for preventing ortreating a Borrelia infection or Lyme disease in a subject, the methodcomprising the step of administering an antibody or fragment thereof asdescribed herein to the subject in an amount effective to prevent ortreat the Borrelia infection or Lyme disease. In particular aspects, theantibody or fragment thereof is a hyperimmune serum, a hyperimmuneplasma, or a purified immunoglobulin fraction thereof. In other aspects,the antibody or fragment thereof is a purified immunoglobulinpreparation or an immunoglobulin fragment preparation.

The anti-OspA antibodies of the invention, in various aspects, areemployed in any known assay method, such as competitive binding assays,direct and indirect sandwich assays, and immunoprecipitation assays(Sola, Monoclonal Antibodies: A Manual of Techniques, pp. 147-158 (CRCPress, Inc., 1987)) for the detection and quantitation of OspApolypeptides. The antibodies will bind OspA polypeptides with anaffinity which is appropriate for the assay method being employed.

For diagnostic or clinical applications, in certain embodiments,anti-OspA antibodies are labeled with a detectable moiety. Thedetectable moiety can be any one which is capable of producing, eitherdirectly or indirectly, a detectable signal. For example, in certainaspects, the detectable moiety is a radioisotope, such as 3H, 14C, 32P,35S, or 125I; a fluorescent or chemiluminescent compound, such asfluorescein isothiocyanate, rhodamine, or luciferin; or an enzyme, suchas alkaline phosphatase, β-galactosidase, or horseradish peroxidase(Bayer et al., Meth. Enzym. 184:138-163 (1990)).

Competitive binding assays rely on the ability of a labeled standard(e.g., an OspA polypeptide, or an immunologically reactive portionthereof) to compete with the test sample analyte (an OspA polypeptide)for binding with a limited amount of anti-OspA antibody. The amount ofan OspA polypeptide in the test sample is inversely proportional to theamount of standard that becomes bound to the antibodies. To facilitatedetermining the amount of standard that becomes bound, the antibodiestypically are insolubilized before or after the competition, so that thestandard and analyte that are bound to the antibodies are convenientlyseparated from the standard and analyte which remain unbound.

Sandwich assays typically involve the use of two antibodies, eachcapable of binding to a different immunogenic portion, or epitope, ofthe protein to be detected and/or quantitated. In a sandwich assay, thetest sample analyte is typically bound by a first antibody which isimmobilized on a solid support, and thereafter a second antibody bindsto the analyte, thus forming an insoluble three-part complex. See, e.g.,U.S. Pat. No. 4,376,110. The second antibody itself, in some instances,is labeled with a detectable moiety (direct sandwich assays) or ismeasured using an anti-immunoglobulin antibody that is labeled with adetectable moiety (indirect sandwich assays). For example, one type ofsandwich assay is an enzyme-linked immunosorbent assay (ELISA), in whichcase the detectable moiety is an enzyme.

The anti-OspA antibodies are also useful for in vivo imaging. Anantibody labeled with a detectable moiety, in certain aspects, isadministered to an animal into the bloodstream, and the presence andlocation of the labeled antibody in the host is assayed. The antibody,in various aspects, is labeled with any moiety that is detectable in ananimal, whether by nuclear magnetic resonance, radiology, or otherdetection means known in the art. In some aspects of the invention, OspAantibodies are used as therapeutics.

Chimeric OspA Compositions and Administration

To administer OspA chimeric polypeptides described herein to subjects,OspA polypeptides are formulated in a composition comprising one or morepharmaceutically acceptable carriers. The phrase “pharmaceutically orpharmacologically acceptable” refers to molecular entities andcompositions that do not produce allergic, or other adverse reactionswhen administered using routes well-known in the art, as describedbelow. “Pharmaceutically acceptable carriers” include any and allclinically useful solvents, dispersion media, coatings, antibacterialand antifungal agents, isotonic and absorption delaying agents and thelike. In some aspects, the composition forms solvates with water orcommon organic solvents. Such solvates are included as well.

The immunogenic composition or vaccine composition of the invention is,in various aspects, administered orally, topically, transdermally,parenterally, by inhalation spray, vaginally, rectally, or byintracranial injection. The term parenteral as used herein includessubcutaneous injections, intravenous, intramuscular, intracisternalinjection, or infusion techniques. Administration by intravenous,intradermal, intramusclar, intramammary, intraperitoneal, intrathecal,retrobulbar, intrapulmonary injection and or surgical implantation at aparticular site is contemplated as well. Generally, compositions areessentially free of pyrogens, as well as other impurities that could beharmful to the recipient.

Formulation of the pharmaceutical composition will vary according to theroute of administration selected (e.g., solution, emulsion). Anappropriate composition comprising the composition to be administered isprepared in a physiologically acceptable vehicle or carrier. Forsolutions or emulsions, suitable carriers include, for example, aqueousor alcoholic/aqueous solutions, emulsions or suspensions, includingsaline and buffered media. Parenteral vehicles, in some aspects, includesodium chloride solution, Ringer's dextrose, dextrose and sodiumchloride, lactated Ringer's or fixed oils. Intravenous vehicles, incertain aspects, include various additives, preservatives, or fluid,nutrient or electrolyte replenishers.

Pharmaceutical compositions useful in the compounds and methods of thepresent invention containing OspA polypeptides as an active ingredientcontain, in various aspects, pharmaceutically acceptable carriers oradditives depending on the route of administration. Examples of suchcarriers or additives include water, a pharmaceutical acceptable organicsolvent, collagen, polyvinyl alcohol, polyvinylpyrrolidone, acarboxyvinyl polymer, carboxymethylcellulose sodium, polyacrylic sodium,sodium alginate, water-soluble dextran, carboxymethyl starch sodium,pectin, methyl cellulose, ethyl cellulose, xanthan gum, gum Arabic,casein, gelatin, agar, diglycerin, glycerin, propylene glycol,polyethylene glycol, Vaseline, paraffin, stearyl alcohol, stearic acid,human serum albumin (HSA), mannitol, sorbitol, lactose, apharmaceutically acceptable surfactant and the like. Additives used arechosen from, but not limited to, the above or combinations thereof, asappropriate, depending on the dosage form of the present invention.

A variety of aqueous carriers, e.g., water, buffered water, 0.4% saline,0.3% glycine, or aqueous suspensions contain, in various aspects, theactive compound in admixture with excipients suitable for themanufacture of aqueous suspensions. Such excipients are suspendingagents, for example sodium carboxymethylcellulose, methylcellulose,hydroxypropylmethylcellulose, sodium alginate, polyvinylpyrrolidone, gumtragacanth and gum acacia; dispersing or wetting agents, in someinstances, are a naturally-occurring phosphatide, for example lecithin,or condensation products of an alkylene oxide with fatty acids, forexample polyoxyethylene stearate, or condensation products of ethyleneoxide with long chain aliphatic alcohols, for exampleheptadecaethyl-eneoxycetanol, or condensation products of ethylene oxidewith partial esters derived from fatty acids and a hexitol such aspolyoxyethylene sorbitol monooleate, or condensation products ofethylene oxide with partial esters derived from fatty acids and hexitolanhydrides, for example polyethylene sorbitan monooleate. The aqueoussuspensions, in some aspects, contain one or more preservatives, forexample ethyl, or n-propyl, p-hydroxybenzoate.

In some aspects, OspA compositions are lyophilized for storage andreconstituted in a suitable carrier prior to use. This technique hasbeen shown to be effective with conventional immunoglobulins. Anysuitable lyophilization and reconstitution techniques known in the artare employed. It is appreciated by those skilled in the art thatlyophilization and reconstitution leads to varying degrees of antibodyactivity loss and that use levels are often adjusted to compensate.

Dispersible powders and granules suitable for preparation of an aqueoussuspension by the addition of water provide the active compound inadmixture with a dispersing or wetting agent, suspending agent and oneor more preservatives. Suitable dispersing or wetting agents andsuspending agents are exemplified by those already mentioned above.

In certain aspects, the concentration of OspA in these formulationsvaries widely, for example from less than about 0.5%, usually at or atleast about 1% to as much as 15 or 20% by weight and will be selectedprimarily based on fluid volumes, viscosities, etc., in accordance withthe particular mode of administration selected. Thus, for example, andwithout limitation, a typical pharmaceutical composition for parenteralinjection is made up to contain 1 ml sterile buffered water, and 50 mgof blood clotting factor. A typical composition for intravenous infusioncould be made up to contain 250 ml of sterile Ringer's solution, and 150mg of blood clotting factor. Actual methods for preparing parenterallyadministrable compositions are known or are apparent to those skilled inthe art and are described in more detail in, for example, Remington'sPharmaceutical Science, 15th ed., Mack Publishing Company, Easton, Pa.(1980). An effective dosage is usually within the range of 0.01 mg to1000 mg per kg of body weight per administration.

In various aspects, the pharmaceutical compositions are in the form of asterile injectable aqueous, oleaginous suspension, dispersions orsterile powders for the extemporaneous preparation of sterile injectablesolutions or dispersions. The suspension, in some aspects, is formulatedaccording to the known art using those suitable dispersing or wettingagents and suspending agents which have been mentioned above. Thesterile injectable preparation, in certain aspects, is a sterileinjectable solution or suspension in a non-toxic parenterally-acceptablediluent or solvent, for example as a solution in 1,3-butane diol. Insome embodiments, the carrier is a solvent or dispersion mediumcontaining, for example, water, ethanol, polyol (for example, glycerol,propylene glycol, and liquid polyethylene glycol, and the like),suitable mixtures thereof, vegetable oils, Ringer's solution andisotonic sodium chloride solution. In addition, sterile, fixed oils areconventionally employed as a solvent or suspending medium. For thispurpose any bland fixed oil is employed, in various aspects, includingsynthetic mono- or diglycerides. In addition, fatty acids such as oleicacid find use in the preparation of injectables.

In all cases the form must be sterile and must be fluid to the extentthat easy syringability exists. The proper fluidity is maintained, forexample, by the use of a coating, such as lecithin, by the maintenanceof the required particle size in the case of dispersion and by the useof surfactants. It must be stable under the conditions of manufactureand storage and must be preserved against the contaminating action ofmicroorganisms, such as bacteria and fungi. The prevention of the actionof microorganisms is brought about by various antibacterial andantifungal agents, for example, parabens, chlorobutanol, phenol, sorbicacid, thimerosal, and the like. In many cases, it will be desirable toinclude isotonic agents, for example, sugars or sodium chloride. Incertain aspects, prolonged absorption of the injectable compositions isbrought about by the use in the compositions of agents delayingabsorption, for example, aluminum monostearate and gelatin.

Compositions useful for administration, in certain aspects, areformulated with uptake or absorption enhancers to increase theirefficacy. Such enhancers, include, for example, salicylate,glycocholate/linoleate, glycholate, aprotinin, bacitracin, SDS, caprateand the like. See, e.g., Fix (J. Pharm. Sci., 85:1282-1285, 1996) andOliyai et al. (Ann. Rev. Pharmacol. Toxicol., 32:521-544, 1993).

In addition, the properties of hydrophilicity and hydrophobicity of thecompositions used in the compounds and methods of the invention are wellbalanced, thereby enhancing their utility for both in vitro andespecially in vivo uses, while other compositions lacking such balanceare of substantially less utility. Specifically, compositions in theinvention have an appropriate degree of solubility in aqueous mediawhich permits absorption and bioavailability in the body, while alsohaving a degree of solubility in lipids which permits the compounds totraverse the cell membrane to a putative site of action.

In particular aspects, the OspA polypeptides described herein areformulated in a vaccine composition comprising adjuvant. Any adjuvantknown in the art is used in various aspects of the vaccine composition,including oil-based adjuvants such as Freund's Complete Adjuvant andFreund's Incomplete Adjuvant, mycolate-based adjuvants (e.g., trehalosedimycolate), bacterial lipopolysaccharide (LPS), peptidoglycans (i.e.,mureins, mucopeptides, or glycoproteins such as N-Opaca, muramyldipeptide [MDP], or MDP analogs), proteoglycans (e.g., extracted fromKlebsiella pneumoniae), streptococcal preparations (e.g., OK432),Biostim™ (e.g., 01K2), the “Iscoms” of EP 109 942, EP 180 564 and EP 231039, aluminum hydroxide, saponin, DEAE-dextran, neutral oils (such asmiglyol), vegetable oils (such as arachis oil), liposomes, Pluronic®polyols, the Ribi adjuvant system (see, for example GB-A-2 189 141), orinterleukins, particularly those that stimulate cell mediated immunity.An alternative adjuvant consisting of extracts of Amycolata, a bacterialgenus in the order Actinomycetales, has been described in U.S. Pat. No.4,877,612. Additionally, proprietary adjuvant mixtures are commerciallyavailable. The adjuvant used depends, in part, on the recipient subject.The amount of adjuvant to administer depends on the type and size of thesubject. Optimal dosages are readily determined by routine methods.

The vaccine composition optionally includes vaccine-compatiblepharmaceutically acceptable (i.e., sterile and non-toxic) liquid,semisolid, or solid diluents that serve as pharmaceutical vehicles,excipients, or media. Any diluent known in the art is used. Exemplarydiluents include, but are not limited to, polyoxyethylene sorbitanmonolaurate, magnesium stearate, methyl- and propylhydroxybenzoate,talc, alginates, starches, lactose, sucrose, dextrose, sorbitol,mannitol, gum acacia, calcium phosphate, mineral oil, cocoa butter, andoil of theobroma.

The vaccine composition is packaged in forms convenient for delivery.The compositions are enclosed within a capsule, caplet, sachet, cachet,gelatin, paper, or other container. These delivery forms are preferredwhen compatible with entry of the immunogenic composition into therecipient organism and, particularly, when the immunogenic compositionis being delivered in unit dose form. The dosage units are packaged,e.g., in tablets, capsules, suppositories, vials, or cachets.

The invention includes methods for inducing an immunological response ina subject, including OspA antibodies in a mammalian host comprisingadministering an effective amount of the Osp A compositions describedherein. Likewise, the invention includes methods for preventing ortreating a Borrelia infection or Lyme disease in a subject, the methodcomprising the step of administering an effective amount of the vaccinecompositions described herein to the subject.

The vaccine composition is introduced into the subject to be immunizedby any conventional method as described herein in detail above. Incertain aspects, the composition is administered in a single dose or aplurality of doses over a period of time (as described in more detailbelow).

Dosing of a Chimeric OspA Composition/Methods for Inducing anImmunological Response

The useful dosage of immunogenic composition or vaccine composition tobe administered will vary depending on various factors which modify theaction of drugs, e.g. the age, condition, body weight, sex and diet ofthe subject, the severity of any infection, time of administration, modeof administration, and other clinical factors.

In some aspects, formulations or compositions of the invention areadministered by an initial bolus followed by booster delivery after aperiod of time has elapsed. In certain aspects, formulations of theinvention are administered by an initial bolus followed by a continuousinfusion to maintain therapeutic circulating levels of drug product. Inparticular aspects, immunogenic compositions or vaccine compositions ofthe invention are administered in a vaccination scheme after variousperiods of time. In some aspects, the vaccination is delivered in arapid immunization scheme for travelers to regions that are prone toBorrelia infection. As another example, the composition or formulationof the invention is administered as a one-time dose. Those of ordinaryskill in the art readily optimize effective dosages and administrationregimens as determined by good medical practice and the clinicalcondition of the individual subject. The frequency of dosing depends onthe pharmacokinetic parameters of the agents and the route ofadministration.

The pharmaceutical formulation is determined by one skilled in the artdepending upon the route of administration and desired dosage. See forexample, Remington's Pharmaceutical Sciences, 18th Ed. (1990, MackPublishing Co., Easton, Pa. 18042) pages 1435-1712, the disclosure ofwhich is hereby incorporated by reference. Such formulations, in someinstances, influence the physical state, stability, rate of in vivorelease, and rate of in vivo clearance of the administered composition.Depending on the route of administration, a suitable dose is calculated,in particular aspects, according to body weight, body surface area ororgan size. In some aspects, appropriate dosages are ascertained throughuse of established assays for determining blood level dosages inconjunction with appropriate dose-response data. In certain aspects, theantibody titer of an individual is measured to determine optimal dosageand administration regimens. The final dosage regimen will be determinedby the attending doctor or physician, considering various factors whichmodify the action of the pharmaceutical compositions, e.g. thecomposition's specific activity, the responsiveness of the subject, theage, condition, body weight, sex and diet of the subject, the severityof any infection or malignant condition, time of administration andother clinical factors. As studies are conducted, further informationwill emerge regarding the appropriate dosage levels and duration oftreatment for the prevention and/or treatment of relevant conditions.

In certain aspects, the OspA immunogenic or vaccine compositioncomprises any dose of OspA nucleic acid molecule(s) or polypeptide(s)sufficient to evoke an immune response in the subject. The effectiveamount of an OspA immunogenic or vaccine composition to be employedtherapeutically will depend, for example, upon the therapeutic contextand objectives. One skilled in the art will appreciate that theappropriate dosage levels for vaccination or treatment will thus varydepending, in part, upon the molecule delivered, the indication forwhich the OspA molecule(s) are being used, the route of administration,and the size (body weight, body surface or organ size) and condition(the age and general health) of the patient. Accordingly, the clinician,in some instances, titers the dosage and modifies the route ofadministration to obtain the optimal therapeutic effect.

A typical dosage, in various aspects, ranges from about 0.1 μg/kg to upto about 100 mg/kg or more, depending on the factors mentioned above. Inother embodiments, the dosage may range from 0.1 μg/kg up to about 100mg/kg; or 1 μg/kg up to about 100 mg/kg; or 5 μg/kg up to about 100mg/kg. By way of example, a dose of a OspA polypeptide useful in thepresent invention is approximately 10 μg/ml, 20 μg/ml, 30 μg/ml, 40μg/ml, 50 μg/ml, 60 μg/ml, 70 μg/ml, 80 μg/ml, 90 μg/ml, 100 μg/ml, 110μg/ml, 120 μg/ml, 130 μg/ml, 140 μg/ml, 150 μg/ml, 160 μg/ml, 170 μg/ml,180 μg/ml, 190 μg/ml, 200 μg/ml, 210 μg/ml, 220 μg/ml, 230 μg/ml, 240μg/ml, 250 μg/ml, 260 μg/ml, 270 μg/ml, 280 μg/ml, 290 μg/ml, 300 μg/ml,320 μg/ml, 340 μg/ml, 360 μg/ml, 380 μg/ml, 400 μg/ml, 420 μg/ml, 440μg/ml, 460 μg/ml, 480 μg/ml, 500 μg/ml, 520 μg/ml, 540 μg/ml, 560 μg/ml,580 μg/ml, 600 μg/ml, 620 μg/ml, 640 μg/ml, In particular aspects, atypical dose comprises 0.1 to 5.0 ml per subject. In more particularaspects, a typical dose comprises 0.2 to 2.0 ml per subject. In certainaspects, a dose comprises 0.5 to 1.0 ml per subject.

The frequency of dosing will depend upon the pharmacokinetic parametersof the OspA molecule in the formulation used. Typically, a clinicianwill administer the composition until a dosage is reached that achievesthe desired effect. The composition, in various aspects, is thereforeadministered as a single dose, or as two or more doses (which may or maynot contain the same amount of the desired molecule) over time, or as acontinuous infusion via an implantation device or catheter. Furtherrefinement of the appropriate dosage is routinely made by those ofordinary skill in the art and is within the ambit of tasks routinelyperformed by them. Appropriate dosages are often ascertained through useof appropriate dose-response data which is routinely obtained.

Kits

As an additional aspect, the invention includes kits which comprise oneor more pharmaceutical formulations for administration of OspApolypeptide(s) to a subject packaged in a manner which facilitates theiruse for administration to subjects.

In a specific embodiment, the invention includes kits for producing asingle dose administration unit. The kits, in various aspects, eachcontain both a first container having a dried protein and a secondcontainer having an aqueous formulation. Also included within the scopeof this invention are kits containing single and multi-chamberedpre-filled syringes (e.g., liquid syringes and lyosyringes).

In another embodiment, such a kit includes pharmaceutical formulationdescribed herein (e.g., a composition comprising a therapeutic proteinor peptide), packaged in a container such as a sealed bottle or vessel,with a label affixed to the container or included in the package thatdescribes use of the compound or composition in practicing the method.In one embodiment, the pharmaceutical formulation is packaged in thecontainer such that the amount of headspace in the container (e.g., theamount of air between the liquid formulation and the top of thecontainer) is very small. Preferably, the amount of headspace isnegligible (i.e., almost none).

In one aspect, the kit contains a first container having a therapeuticprotein or peptide composition and a second container having aphysiologically acceptable reconstitution solution for the composition.In one aspect, the pharmaceutical formulation is packaged in a unitdosage form. The kit optionally further includes a device suitable foradministering the pharmaceutical formulation according to a specificroute of administration. In some aspects, the kit contains a label thatdescribes use of the pharmaceutical formulations.

Each publication, patent application, patent, and other reference citedherein is incorporated by reference in its entirety to the extent thatit is not inconsistent with the present disclosure.

It is understood that the examples and embodiments described herein arefor illustrative purposes only and that various modifications or changesin light thereof will be suggested to persons skilled in the art and areto be included within the spirit and purview of this application andscope of the appended claims. All publications, patents, and patentapplications cited herein are hereby incorporated by reference in theirentirety for all purposes.

EXAMPLES

Additional aspects and details of the invention will be apparent fromthe following examples, which are intended to be illustrative ratherthan limiting.

Example 1 Analysis of the Sequence of OspA from European BorreliaBurgdorferi Sensu Lato Strains (Molecular Epidemiology) for theDetermination of an OspA Vaccine Formulation

The objective of the study was to determine a suitable formulation for aLyme disease OspA vaccine for Europe. The study was based on sequenceanalysis of the OspA gene (molecular epidemiology) from a large anddiverse strain collection of B. burgdorferi sensu lato, which adequatelyrepresents a broad geographic coverage of Europe, the various clinicalsyndromes associated with disease, and each of the three pathogenicgenospecies (B. afzelii, B. garinii and B. burgdorferi ss) associatedwith Lyme disease. Lyme disease is caused by Borrelia burgdorferi sensulato, which comprises 13 genospecies in total, three of which (B.afzelii, B. garinii and B. burgdorferi ss) are recognized as beingpathogenic in humans.

At the outset, a large scale epidemiological study (see Table 3 below)was carried out which evaluated Borrelia burgdoferi sensu lato strainsfrom patients with Lyme disease (and from ticks) from 21 countries inEurope. A total of 553 European Borrelia isolates collected from 16European countries were studied. Each species was determined by PCRusing primer sets specific for the 16s rRNA genes of each species.

Isolates from each of the three Borrelia species known to cause humanLyme disease in Europe were well represented: B. afzelii (n=309, 55.9%),B. burgdorferi sensu stricto (n=67, 12.1%), and B. garinii (n=173,31.3%). Of the 359 human isolates, 56.8% were B. afzelii and B. afzeliiwas the predominant species determined from human isolates in mostlocations. Similarly, B. afzelii was isolated from 54.1% of tickisolates. B. burgdorferi s.s. was isolated from 11.7% of human strainsand 12.9% of tick isolates. B. burgdorferi s.s. was isolated from humanisolates from South Eastern Europe, notably Italy, Hungary, Slovenia andAustria. B. garinii strains were isolated from 30.4% of human isolatesand accounted for 33% of tick isolates. B. garinii strains isolated fromhumans and ticks were obtained from most of the geographic regionsthroughout Europe. The data from this study correlated well with thedata presented from other European studies and suggests that thecollection of isolates studied represents an accurate picture of Lymedisease in Europe.

OspA sequencing was carried out to determine an optimal vaccineformulation for Europe. Based on this data, a vaccine including OspAtypes 1 to 6 would cover 98.1% of the strains and 96.7% of invasivedisease cases. Epidemiological study results of European Borreliaisolates indicate that a vaccine based on OspA types 1, 2, 3, 4, 5 and 6would provide theoretical coverage in Europe of 98% of Lyme disease and96.7% of invasive neuroborreliosis isolates.

TABLE 3 Epidemiological Study Results Isolates from Vaccine invasiveVaccine coverage disease coverage of invasive OspA type Human isolatescases total¹ disease² B. afzelii type 2  56.8% (204)  3% (7) 56.8% 11.7%B. b s.s. type 1 11.7% (42) 17% (7) 68.5% 23.3% B. garinii type 6 15.9%(57)  40% (23) 84.4% 61.7% B. garinii type 5  7.2% (26) 35% (9) 91.6%76.7% B. garinii type 4  4.5% (16) 44% (7) 96.1% 88.3% B. garinii Vtype3 2.0% (7) 71% (5) 98.1% 96.7% B. garinii type 7 0.8% (3) 67% (2) 98.9% 100% B. spielmanii 1.1% (4) 0%  100% ¹Predicted vaccine coverage basedon numbers of isolates; totals are cumulative. ²Predicted vaccinecoverage of isolates from cases of neuroborreliosis; totals arecumulative.

Hence a vaccine comprising three novel recombinant OspAs (1/2, 6/4, and5/3), each representing 2 OspA serotypes, would retain key structuralelements necessary for protection against all 6 prevalent OspA serotypes(1-6) associated with Lyme borreliosis in Europe and against the singleOspA serotype associated with Lyme borreliosis in the USA.

Inclusion of an OspA 5/3 construct, representing B. garinii OspAserotypes 5 and 3, (together with OspA serotypes 1/2 and 6/4), shouldprotect against 98.1% of disease and 96.7% of invasive isolates. Avaccine without OspA 5/3 would be expected to protect against only about88.9% of disease, and only about 73.4% of invasive disease. Thus, avaccine comprising all six serotypes is more effective in the preventionof Lyme disease than a vaccine with only four serotypes.

Example 2 Strategy for the Construction of Synthetic OspA Genes EncodingLipidated OspA

The aim of the study was to prepare lipidated OspA chimeric constructsfrom several strains of Borrelia in order to make a vaccine that wouldprotect the recipient from Lyme disease caused by any of these severalstrains of Borrelia. The general strategy is summarized in FIG. 1 and isdescribed below.

For each novel OspA gene, four sets of oligonucleotides of between 30-60bases were synthesized. Each oligonucleotide set consisted of between8-12 complementary overlapping oligonucleotides. The oligonucleotidesfrom each set were annealed together, in separate experiments, togenerate double-stranded DNA fragments with specific restriction enzymerecognition sites at either end, i.e. fragments N-H (Nde I-Hind III),H-K (Hind III-Kpn I), K-E (Kpn I-EcoR I) and E-B (EcoR I-BamH I). Eachof the four fragments was cloned independently into pUC18, cut with thecorresponding restriction enzymes and transformed into the E. coli hostDH5α, after which the sequence of the cloned fragment was verified.

E. coli strain DH5α [genotype: end A1 hsdR17 (r_(K) ⁻m_(K) ⁺) supE44thi-1 recA1 gyrA (Nal^(r)) relA1 Δ(lacZYA-argF)U169 deoR(Φ80dlacΔ(lacZ)M15] (Gibco BRL) was used for all intermediate cloningsteps. This strain is derived from E. coli strain K12, one of the mostwidely used hosts in genetic engineering. The strain is amp⁻ to allowselection of transformants with vectors containing the ampicillinresistance gene (amp). E. coli HMS174(DE3) was selected as the host forexpression. E. coli HMS174(DE3) host cells [genotype: F-recA1 hsdR(r_(k12) ⁻m_(k12) ⁺) Rif^(R) (DE3)](Novagen) were used for the finalcloning steps. The strain is kan⁻ to allow selection of transformantswith vectors containing the kanamycin resistance gene (kan).

pUC18 (Gibco BRL, Basel, Switzerland) was used as the cloning vector forall intermediate steps, because genetic manipulations and sequencingwere easier with this plasmid than with pET30a. The principal featuresare notably, the lacZ gene fragment coding for LacZ alpha peptide frombase pairs 149 to 469 (lac promoter at base pairs 507), the bla geneencoding the ampicillin resistance determinant from base pairs 1629 to2486 (bla promoter at base pairs 2521), the origin of replication atbase pairs 867 and multiple cloning sites from base pairs 185 to 451(FIG. 12).

pET30a (Novagen) was used as the expression vector for the finalcomplete OspA gene insert. In pET vectors genes are cloned under thecontrol of a T7 promoter and expression is induced by providing a sourceof T7 RNA polymerase in the host cell (no expression occurs until asource of T7 RNA polymerase is provided). The principal features are thegene encoding kanamycin resistance (kan) at base pairs 4048 to 4860, thelacI gene base pairs 826-1905, the F1 origin of replication at basepairs 4956-5411 and multiple cloning sites from base pairs 158 to 346(FIG. 13).

The four fragments needed to make a full-length OspA gene were excisedfrom a DNA miniprep. DNA was isolated from each of the four clones usingthe same restriction enzymes used for the original cloning step. The DNAfragments were purified and ligated together with pUC18 DNA cut with NdeI and BamH I and were transformed into E. coli DH5α competent cells. Thefull-length OspA gene cloned in pUC18 was sequenced to confirm that noerrors had been introduced in this step.

The OspA gene was then sub-cloned into a pET-30a expression vector usingthe restriction enzymes Nde I and BamH I and transformed into the E.coli host HMS 174(DE3). In the pET30a vector, the OspA gene iscontrolled by the bacteriophage T7 promoter.

Three synthetic OspA genes were designed to encode OspA molecules withthe protective epitopes from serotype 1 and 2 OspAs (lipB sOspA 1/2²⁵¹),serotype 6 and 4 OspAs (lipB sOspA 6/4) and serotype 5 and 3 OspAs (lipBsOspA 5/3) of Borrelia. The primary amino acid sequences of thesemolecules (SEQ ID NOS: 2, 4, and 6, respectively) are shown in FIGS. 2-8and described herein with a full description of the main featuresincorporated into their design.

The oligonucleotides for the lipB sOspA 1/2 construct were synthesizedin-house on an ABI 394 DNA/RNA synthesizer. The oligonucleotides for thelipB sOspA 5/3 and lipB sOspA 6/4 constructs were purchased fromGenXpress (Wiener Neudorf, Austria) and were HPLC purified.

TABLE 4  Oligonucleotides for lipB sOspA 1/2* gene fragments SEQ ID NameSequence (5′-3′) L S NO Hin dIII-Kpn I fragment NH1TATGCGTCTGTTGATCGGCTTTGCTCTGGCGCTGGCTCTGATCGG 45 C 59 NH2CTGCGCACAGAAAGGTGCTGAGTCTATTGGTTCCGTTTCTGTAGATCTGC 50 C 60 NH3CCGGTGAAATGAAGGTTCTGGTGAGCAAAGAAAAAGACAAGAACGGCAAG 50 C 61 NH4TACGATCTCATCGCAACCGTCGACAAGCTGGAGCTGAAAGGTACTTCTGA 50 C 62 NH5TAAAAACAACGGCTCTGGTGTGCTGGAGGGCGTCAAAACTAACAAGAGCAAAGTAA 56 C 63 NH6AGCTTTACTTTGCTCTTGTTAGTTTTGACGCCCTCCAGCA 40 C′ 64 NH7CACCAGAGCCGTTGTTTTTATCAGAAGTACCTTTCAGCTCCAGCTTGTCG 50 C′ 65 NH8ACGGTTGCGATGAGATCGTACTTGCCGTTCTTGTCTTTTTCTTTGCTCAC 50 C′ 66 NH9CAGAACCTTCATTTCACCGGGCAGATCTACAGAAACGGAACCAATAGACT 50 C′ 67 NH10CAGCACCTTTCTGTGCGCAGCCGATCAGAGCCAGCGCCAGAGCAAAGCCGATCAACA 63 C′ 68GACGCA Hin dIII-Kpn I fragment HK1 AGCTTACGATCTCTGACGATCTCGGTCAGACCAC 34C 69 HK2 GCTGGAAGTTTTCAAAGAGGATGGCAAGACCCTCGTGTCCAAAAAAGTAA 50 C 70 HK3CTTCCAAAGACAAGTCCTCTACGGAAGAAAAATTCAACGAAAAAGGTGAG 50 C 71 HK4GTGTCTGAAAAGATCATCACCATGGCAGACGGCACCCGTC 40 C 72 HK5TTGAATACACCGGTATTAAAAGCGATGGTAC 31 C 73 HK6CATCGCTTTTAATACCGGTGTATTCAAGACGGGTGCCGTCTGCCATG 47 C′ 74 HK7GTGATGATCTTTTCAGACACCTCACCTTTTTCGTTGAATTTTTCTTCCGT 50 C′ 75 HK8AGAGGACTTGTCTTTGGAAGTTACTTTTTTGGACACGAGGGTCTTGCCAT 50 C′ 76 HK9CCTCTTTGAAAACTTCCAGCGTGGTCTGACCGAGATCGTCAGAGATCGTA 40 C′ 77Kpn I-EcoR I fragment KE1 CGGTAAAGCGAAATATGTTCTGAAAAACTTCACTCTGGA 39 C78 KE2 AGGCAAAGTGGCTAATGATAAAACCACCTTGGAAGTCAAGGAAGGCACCG 50 C 79 KE3TTACTCTGAGCATGAATATCTCCAAATCTGGTGAAGTTTCCGTTGAACTG 50 C 80 KE4AACGACACTGACAGCAGCGCTGCGACTAAAAAAACTGCAGCGTGG 45 C 81 KE5AATTCCACGCTGCAGTTTTTTTAGTCGCA 29 C′ 82 KE6GCGCTGCTGTCAGTGTCGTTCAGTTCAACGGAAACTTCACCAGATTTGGA 50 C′ 83 KE7GATATTCATGCTCAGAGTAACGGTGCCTTCCTTGACTTCCAAGGTGGTTT 50 C′ 84 KE8TATCATTAGCCACTTTGCCTTCCAGAGTGAAGTTTTTCAGAACATATTTCGCTTTACCGG 63 C′ 85TAC EcoR I-BamH I fragment EB1AATTCCAAAACTTCTACTTTAACCATTAGCGTTAACAGCAAAAAA 45 C 86 EB2ACTACCCAGCTGGTGTTCACTAAACAAGACACGATCACTGTGCAGAAATA 50 C 87 EB3CGACTCCAACGGCACCAACTTAGAAGGCACGGCAGTCGAAATTAAAACCC 50 C 88 EB4TTGATGAACTGAAAAACGCGCTGAAATAAGCTGAGCG 40 C 89 EB5GATCCGCTCAGCTTATTTCAGCGCGTTTTTCAGTTCATCAAGGGTTTTAATTTCGACTG 60 C′ 90 CCEB6 GTGCCTTCTAAGTTGGTGCCGTTGGAGTCGTATTTCTGCACAGTGATCGT 50 C′ 91 EB7GTCTTGTTTAGTGAACACCAGCTGGGTAGTTTTTTTGCTGTTAACGCTAA 50 C′ 92 EB8TGGTTAAAGTAGAAGTTTTGG 21 C′ 93 *A single amino acid change wasintroduced by PCR, lipB sOspA 1/2 was the name of the construct beforethe introduced change and lipB sOspA 1/2²⁵¹ was the name after theintroduced change. L Length of oligonucleotide in bases S Strand, C(coding) or complementary (C′)

TABLE 5  Oligonucleotides for lipB sOspA 5/3 gene fragments SEQ ID NameSequence (5′-3′) L S NO Nde I-Hin dIII fragment N51TATGCGTCTGTTGATCGGCTTTGCTTTGGCGCTGGCTTTAATCGGCTG 48 C  94 N52TGCACAGAAAGGTGCTGAGTCTATTGGTTCCGTTTCTGTAGATCTGCCCG 50 C  95 N53GGGGTATGAAAGTTCTGGTAAGCAAAGAAAAAGACAAAAACGGTAAATAC 50 C  96 N54AGCCTGATGGCAACCGTAGAAAAGCTGGAGCTTAAAGGCACTTCTGATAA 50 C  97 N55AAACAACGGTTCTGGCACCCTGGAAGGTGAAAAAACTAACAAAAGCAAAGTAA 53 C  98 N56AGCTTTACTTTGCTTTTGTTAGTTTTTTCACCTTCCA 37 C′  99 N57GGGTGCCAGAACCGTTGTTTTTATCAGAAGTGCCTTTAAGCTCCAGCTTT 50 C′ 100 N58TCTACGGTTGCCATCAGGCTGTATTTACCGTTTTTGTCTTTTTCTTTGCT 50 C′ 101 N59TACCAGAACTTTCATACCCCCGGGCAGATCTACAGAAACGGAACCAATAG 50 C′ 102 N510ACTCAGCACCTTTCTGTGCACAGCCGATTA 30 C′ 103 N511AAGCCAGCGCCAAAGCAAAGCCGATCAACAGACGCA 36 C′ 104 Hin dIII-Kpn I fragmentH51 AGCTTACTATTGCTGAGGATCTGAGCAAAACCACCTTTGAAATCTTC 47 C 105 H52AAAGAAGATGGCAAAACTCTGGTATCTAAAAAAGTAACCCTGAAAGACAA 50 C 106 H53GTCTTCTACCGAAGAAAAATTCAACGAAAAGGGTGAAATC 40 C 107 H54TCTGAAAAAACTATCGTAATGGCAAATGGTAC 32 C 108 H55AAGGTGGTTTTGCTCAGATCCTCAGCAATAGTA 33 C′ 109 H56AGAGTTTTGCCATCTTCTTTGAAGATTTCA 30 C′ 110 H57ATTTTTCTTCGGTAGAAGACTTGTCTTTCAGGGTTACTTTTTTAGATACC 50 C′ 111 H58CATTTGCCATTACGATAGTTTTTTCAGAGATTTCACCCTTTTCGTTGA 48 C′ 112Kpn I-EcoR I fragment K51CCGTCTGGAATACACCGACATCAAAAGCGATAAAACCGGCAAAGCTAA 48 C 113 K52ATACGTTCTGAAAGACTTTACTCTGGAAGGCACTCTGGCTGCTGACGGCA 50 C 114 K53AAACCACTCTGAAAGTTACCGAAGGCACTGTTACTCTGAGCATGAACATT 50 C 115 K54TCTAAATCCGGCGAAATCACCGTTGCACTGGATGACACTGACTCTAGCGG 50 C 116 K55CAATAAAAAATCCGGCACCTGGGATTCTGATACTTCTACTTTAACCATTA 50 C 117 K56GCAAAAACAGCCAGAAAACTAAACAGCTGGG 31 C 118 K57GCTTTTGATGTCGGTGTATTCCAGACGGGTAC 31 C′ 119 K58CCTTCCAGAGTAAAGTCTTTCAGAACGTATTTAGCTTTGCCGGTTTTATC 50 C′ 120 K59CAGTGCCTTCGGTAACTTTCAGAGTGGTTTTGCCGTCAGCAGCCAGAGTG 50 C′ 121 K510CAGTGCAACGGTGATTTCGCCGGATTTAGAAATGTTCATGCTCAGAGTAA 50 C′ 122 K511TCAGAATCCCAGGTGCCGGATTTTTTATTGCCGCTAGAGTCAGTGTCATC 50 C′ 123 K512AATTCCCAGCTGTTTAGTTTTCTGGCTGTTTTTGCTAATGGTTAAAGTAGAAGTA 55 C′ 124EcoR I-BamH I fragment E51 AATTCAAACAGCTGGTATTCACCAAAGAAAACACTATCACCGTAC125 E52 AGAACTATAACCGTGCAGGCAATGCGCTGGAAGGCAGCCC 45 C 126 E53GGCTGAAATTAAAGATCTGGCAGAGCTGAAAGCCGCTTTGAAATAAGCTGAGCG 40 C 127 E54GATCCGCTCAGCTTATTTCAAAGCGGCT 54 C 128 E55TTCAGCTCTGCCAGATCTTTAATTTCAGCCGGGCTGCCTTCCAGCGCATT 28 C′ 129 E56GCCTGCACGGTTATAGTTCTGTACGGTGATAGTGTTTTCTTTGGTGAATACCAGCTGTT 50 C′ 130 TGL Length of oligonucleotide in bases S Strand, C (coding) orcomplementary (C′)

TABLE 6  Oligonucleotides for lipB sOspA 6/4 gene fragments SEQ ID NameSequence (5′-3′) L S NO Nde I-Hin dIII fragment KNH1TATGCGTCTGTTGATCGGCTTTGCTCTGGCGCTGGCTCTGATCGGCTG 131 KNH2CGCACAGAAAGGTGCTGAGTCTATTGGTTCCGTTTCTGTAGATCTGCCCG 48 C 132 KNH3GTGGCATGACCGTTCTGGTCAGCAAAGAAAAAGACAAAAACG 50 C 133 KNH4GTAAATACAGCCTCGAGGCGACCGTCGACA 42 C 134 KNH5AGCTTGTCGACGGTCGCCTCGAGGCTGTATTTACCGTTTTTGTCTTTTTCTTTGCT 30 C 135 KNH6GACCAGAACGGTCATGCCACCGGGCAGATCTACAGAAACG 56 C′ 136 KNH7GAACCAATAGACTCAGCACCTTTCTGTGCGCAGCCGATCAGAGCCAGCGC 40 C′ 137 KNH8CAGAGCAAAGCCGATCAACAGACGCA 50 C′ 138 Hin dIII-Kpn I fragment KHK1AGCTTGAGCTGAAAGGCACCTCTGATAAAAACAACGGTTCCGGCACCCTG 50 C 139 KHK2GAAGGTGAAAAAACTAACAAAAGCAAAGTGAAACTGACCATTGCTGAT 48 C 140 KHK3GACCTCAGCCAGACCAAATTCGAAATTTTCAAAGAAGATGCCAAAACCTT 50 C 141 KHK4AGTATCCAAAAAAGTGACCCTGAAAGACAAGTCCTCTACCGAAGAAAAAT 50 C 142 KHK5TCAACGAAAAGGGTGAAACCTCTGAAAAAACCATCGTAATGGCAAATGGTAC 52 C 143 KHK7CATTTGCCATTACGATGGTTTTTTCAGA 28 C′ 144 KHK8GGTTTCACCCTTTTCGTTGAATTTTTCTTCGGTAGAGGAC 40 C′ 145 KHK9TTGTCTTTCAGGGTCACTTTTTTGGATACTAAGGTTTTGGCATCTTCTTT 50 C′ 146 KHK10GAAAATTTCGAATTTGGTCTGGCTGAGGTCATCAGCAATGGTCAGTTTCA 50 C′ 147 KHK11CTTTGCTTTTGTTAGTTTTTTCACCTTCCAGGGTGCCGGA 40 C′ 148 KHK12ACCGTTGTTTTTATCAGAGGTGCCTTTCAGCTCA 34 C′ 149 Kpn I-EcoR I fragment KKE1CCGTCTGGAATACACCGACATCAAAAGCGATGGCTCCGGCAAAGCCAA 48 C 150 KKE2ATACGTTCTGAAAGACTTCACCCTGGAAGGCACCCTCGCTGCCGACGG 48 C 151 KKE3CAAAACCACCTTGAAAGTTACCGAAGGCACTGTTGTTTTAAG 42 C 152 KKE4CATGAACATCTTAAAATCCGGTGAAATCACCGTTGCGCTG 40 C 153 KKE5GATGACTCTGACACCACTCAGGCCACTAAAAAAACCGGCAAATGGGATTC 50 C 154 KKE6TAACACTTCCACTCTGACCATCAGCGTG 28 C 155 KKE7AATTCACGCTGATGGTCAGAGTGGAAGTGTTAGAATCCCATTTGCCG 47 C′ 156 KKE8GTTTTTTTAGTGGCCTGAGTGGTGTCAGAGTCATCCAGCGCAACGGTGATTTCAC 55 C′ 157 KKE9CGGATTTTAAGATGTTCATGCTTAAAACAACAGTGCCTTCGGTAACTTTC 50 C′ 158 KKE10AAGGTGGTTTTGCCGTCGGCAGCGAGGGTGCCTTCCAGGG 40 C′ 159 KKE11TGAAGTCTTTCAGAACGTATTTGGCTTTGCCGGAGCCATC 40 C′ 160 KKE12GCTTTTGATGTCGGTGTATTCCAGACGGGTAC 32 C′ 161 EcoR I-BamH I fragment KEB1AATTCCAAAAAAACTAAAAACATCGTGTTCACCAAAGAAGACACCATCACCG 162 KEB2TCCAGAAATACGACTCTGCGGGCACCAACCTCGAAGGCAACGCAGTCGAA 52 C 163 KEB3ATCAAAACCCTGGATGAACTGAAAAACGCTCTGAAATAAGCTGAGCG 50 C 164 KEB4GATCCGCTCAGCTTATTTCAGAGCGTTTTTCAGTTCATCCAGGGTTTTGATTT 47 C 165CGACTGCGTTGCCTTCGA KEB5GGTTGGTGCCCGCAGAGTCGTATTTCTGGACGGTGATGGTGTCTTCTTTG 71 C′ 166 KEB6GTGAACACGATGTTTTTAGTTTTTTTGG 50 C′ 167 L Length of oligonucleotide inbases S Strand, C (coding) or complementary (C′)

Preparation of E. Coli Competent Cells.

A single colony was used to inoculate 5 ml modified LB broth (5.5 gNaCl, 5 g yeast extract, 10 g soya peptone, which was not obtained froman animal or genetically modified plant source—per liter of water). Theculture was incubated until it became turbid, after which the culturewas diluted to a volume of 25 ml with pre-warmed modified LB broth. Theculture was incubated further until it had reached an OD600 nm of 0.2 to0.6 (40-60 min) and was diluted to a volume of 125 ml, transferred to a500 ml flask and incubated until an OD600 nm of 0.6 was reached. Theculture was chilled quickly by gentle shaking for 5 min in an ice bathand the cells were pelleted directly (Beckman centrifuge, 4000 rpm for10 min.), washed carefully with TfBI buffer (Teknova Hollister, Calif.)(30 mM K-acetate, 50 mM MnCl₂, 100 mM KCL, 10 mM CaCl₂ 15% glycerol),resuspended in 5 ml of TfBII (10 mM Na-MOPS, 75 mM CaCl₂, 10 mM KCL, 15%glycerol) and held on ice for 15 min. The cells were then pipetted into100 μl aliquots and were snap frozen directly in dry ice.

Annealing of Oligonucleotide Mixtures to Form OspA Gene Fragments (DeNovo Synthesis).

Three synthetic OspA genes were designed to encode OspA molecules withthe protective epitopes from serotype 1 and 2 OspAs (lipB sOspA 1/2),serotype 6 and 4 OspAs (lipB sOspA 6/4) and serotype 5 and 3 OspAs (lipBsOspA 5/3). For each novel OspA gene (lipidated), four sets ofoligonucleotides of between 30-60 base pairs were synthesized (seeTables 4-6). FIGS. 16-18 show the codon optimized sequences for each ofthe constructs aligned with the nucleotide sequences predicted frompublished sequences). Each oligonucleotide set consisted of between 8-12complementary overlapping oligonucleotides. The oligonucleotides fromeach set were annealed together, in separate experiments, to generatedouble-stranded DNA fragments with specific restriction enzymerecognition sites at either end i.e. fragments N-H (Nde I-Hind III), H-K(Hind III-Kpn I), K-E (Kpn I-EcoR I) and E-B (EcoR I-BamH I).

The lyophilized oligonucleotides were reconstituted with distilledwater, the OD260 nm was measured and the concentration was adjusted to10 μM. For each OspA fragment, 2 μl of each of the oligonucleotides weremixed together with 1 μl of T4 polynucleotide kinase and T4 DNA ligasebuffer (10×) and the mixture was incubated at room temperature for 30minutes to enable phosphorylation of the oligos (for the lipB sOspA 6/4construct this step was omitted as the oligos were alreadyphosphorylated). The mixture was heated to 95° C. for 1 minute(denaturing step) and then the oligos were allowed to anneal by leavingthe mix to cool slowly to room temperature. The annealed mix was useddirectly in ligations, or was stored at −20° C. until further needed.

Cloning of OspA Gene Fragments.

Each of the four fragments required for constructing an individualsynthetic OspA gene was cloned independently into pUC18 and transformedinto the E. coli host DH5α (see FIG. 1).

For each novel OspA gene, four sets of oligonucleotides of between 30-60bases were synthesized. Each oligonucleotide set consisted of between8-12 complementary overlapping oligonucleotides. The oligonucleotidesfrom each set were annealed together, in separate experiments, togenerate double-stranded DNA fragments with specific restriction enzymerecognition sites at either end, i.e. fragments N-H (Nde I-Hind III),H-K (Hind III-Kpn I), K-E (Kpn I-EcoR I) and E-B (EcoR I-BamH I). Eachof the four (4) fragments was cloned independently into pUC18 cut withthe corresponding restriction enzymes and transformed into the E. colihost DH5α, after which the sequence of the cloned fragment was verified.

Plasmid DNA (pUC18) was purified from an overnight E. coli culture (LBbroth) with a QIAGEN plasmid purification system according to themanufacturer's protocol. Vector DNA was then digested with pairs ofrestriction enzymes; Nde I & Hind III, Hind III & Kpn I, Kpn I & EcoR I,EcoR I & BamH I in accordance with the manufacturers' protocols. Thedigested samples were applied to a 0.8% agarose gel andelectrophoretically separated. The linearized vector DNA was excised andeluted using a commercial gel elution kit (QIAquick Gel Extraction Kit,Qiagen) according to the manufacturer's protocol and ligated, using T4DNA ligase, to the annealed oligonucleotide mixture. The ligationproducts were transformed into competent cells of E. coli DH5α andtransformants containing the plasmid were selected on LB agar containingampicillin (100 μg/ml).

The presence of the insert of the expected size in the cloning vector,pUC18, was confirmed by purifying plasmid DNA, digesting the DNA withthe enzymes used for cloning and analyzing the DNA fragments by agarosegel electrophoresis using the procedures previously described. Thecloned DNA fragment was sequenced using purified plasmid DNA as the DNAtemplate and the sequencing primers 5′-TCGGGGCTGGCTTAACTATG-3 (SEQ IDNO: 14) and 5′-GCTTCCGGCTCGTAT (SEQ ID NO:15) (which are in the pUC18vector outside the multiple cloning sites, bp 130-150 and bp 530-515,respectively). Sequence reactions were run on an automatic sequencer(ABI 310). Sequences were edited using SequenceEditor and the sequenceswere imported into Vector NTI for analysis. Only clones with the correctsequences were used as building blocks for constructing full-length OspAgenes.

For the lipB sOspA 5/3 gene a different strategy was employed, since nosuitable unique internal site could be found within the Kpn I-BamH Ifragment and the amino acid sequence did not permit the use of aninternal EcoR I site (see FIG. 14). A Pvu II site exists within the KpnI-BamH I fragment, however there are two Pvu II sites in the pUC18vector which mean direct cloning of the fragments in pUC18 is notpossible. Hence, the oligos for the constructs were designed to have anEcoR I site inserted outside and adjacent to the Pvu II site, to permitcloning of the Kpn I-EcoR I and the EcoR I-BamH I fragments into pUC18.Subsequent digestion of the inserted fragments with Kpn I, EcoR I andBamH I generated fragments, which were subsequently digested with PvuII. The Pvu II-digested fragments (Kpn I-Pvu II and Pvu II-BamH I) werethen used in a triple ligation with pUC18 vector DNA cut with Kpn I andBamH I to generate the Kpn I-BamH I fragment.

Constructing Full-Length OspA Genes.

In the next step, each of the four fragments required for constructingan individual synthetic OspA gene was excised from the pUC18 vector andre-cloned, in a single step, into pUC18 vector to generate a full-lengthOspA gene (see FIG. 1).

The four fragments needed to make full-length genes were excised fromminiprep. DNA isolated using the same restriction enzymes used for theoriginal cloning step. The digested samples were applied to an agarosegel and electrophoretically separated. The DNA for each of therespective 4 insert fragments was excised and eluted using a commercialgel elution kit (QiaQuick Gel Extraction Kit) according to themanufacturer's protocol and ligated, using T4 DNA ligase, to linearizedvector DNA digested with Nde I and BamH I and purified using a QIAquickGel Extraction Kit. The ligated DNA was transformed into competent cellsof E. coli DH5α and clones containing the plasmid were selected on LBagar containing ampicillin (100 μg/ml). Colonies were screened by PCRfor the presence of inserts of the expected size (approx 830 bp).

Single colonies were used as template DNA in PCR reactions comprising10× buffer (15 mM Tris-HCl (pH 8.0), 50 mM KCl, 1.5 mM MgCl₂), 200 μMdNTPs, 1.25 U Amplitaq DNA polymerase, 400 nM forward primer5′-TCGGGGCTGGCTTAACTATG-3 (SEQ ID NO: 14) and 400 nM reverse primer5′-GCTTCCGGCTCGTAT (SEQ ID NO: 15). PCR reaction conditions were asfollows; 94° C. for 5 min., 35× (94° C. for 30 s, 48° C. for 30 s, 72°C. for 1 min 30 s) followed by a soak at 72° C. for 5 minutes and a holdat 4° C. PCR products were used directly or stored at ≦□□115° C. untilfurther use. PCR products were analyzed by agarose gel electrophoresisfor the presence of inserts of the correct size (approx. 980 bp).Inserts of the correct size were sequenced to confirm that no errors hadbeen introduced i.e. sequence reactions were set up using plasmid DNAisolated (QIAGEN Plasmid Purification kit) from overnight cultures (LBamp broth) and using sequencing primers that flank the cloning sites(5′-TCGGGGCTGGCTTAACTATG-3′(SEQ ID NO: 14) and5′-GCTTCCGGCTCGTATGTTGT-3′ (SEQ ID NO: 16), bp 130-150 and 530-510,respectively). Sequence reactions were run on an automatic sequencer(ABI 310). Sequences were edited using SequenceEditor and the sequenceswere imported into Vector NTI for analysis.

Sub-Cloning of Novel OspA Genes into the pET30a Expression Vector.

Once the full length OspA gene was verified in pUC18, the OspA geneswere then sub-cloned into the pET-30a expression vector using therestriction enzymes NdeI and BamH I and transformed into the E. colihost HMS 174(DE3).

Miniprep DNA from pUC18 clones with the correct sequence was digestedwith Nde I and BamH I. Similarly pET30a vector DNA was digested with NdeI and BamH I. The digested DNAs were run on an agarose gel andelectrophoretically separated. The insert fragment of approximately 830bp and the linearized vector DNA were excised and purified as describedpreviously. The vector and insert DNA were ligated, using T4 DNA ligaseand the ligation products were transformed into competent cells of E.coli HMS174(DE3) (Novagen). The transformants were plated onto LB platescontaining kanamycin (30 μg/ml). Single colonies were screened by PCRusing the primers 5′-TTATGCTAGTTATTGCTCAGCG-3′ (SEQ ID NO:17) and5′-TTCCCCTCTAGAAATAATTTTGT-3′ (SEQ ID NO: 18). PCR products were appliedto an agarose gel and were electrophoretically separated. Colonies thatyielded a product of the correct size (approx. 1 kb) were subsequentlyused to set up overnight cultures, from which miniprep DNA was isolatedusing a QIAGEN Plasmid Purification kit according to the manufacturer'sprotocol. The sequence was again confirmed (using primers5′-TTATGCTAGTTATTGCTCAGCG-3′ (SEQ ID NO: 17) and5′-TTCCCCTCTAGAAATAATTTTGT-3′ (SEQ ID NO:18), by 65-86 and 395-373,respectively) and colonies were selected for expression testing.

Generating lipB sOspA 1/2²⁵¹ from lipB sOspA 1/2.

A single amino acid was changed in the lipB sOspA 1/2 construct, namelyamino acid alanine at position 251 was changed to an asparagine residue,to enhance immunogenicity. The amino acid change was introduced by PCR.First, PCR was set up with the external forward primer and the internalreverse primer yielding a product of about 730 bp with the introducedamino acid change (see FIG. 15). Second, PCR was set up with theinternal forward primer and the external reverse primer to yield aproduct of 100 bp containing the introduced amino acid change. The twoPCR products, which overlapped in sequence, were then used as templateDNA in a final PCR reaction with the external forward and externalreverse primers to yield the final full-length OspA product containingthe introduced amino acid change.

The pET30a construct was used as the source of template DNA. PCRreactions were set up comprising 10× buffer [15 mM Tris-HCl (pH 8.0), 50mM KCl, 1.5 mM MgCl2], 200 μm dNTPs, 1.25 U Amplitaq DNA polymerase, and400 nM of each primer pair (primer pair 5′-GGA ATT CCA TAT GCG TCT GTTGAT CGG CT (SEQ ID NO: 19) & 5′-TTG GTG CCT GCG GAG TCG (SEQ ID NO:20)and primer pair 5′-AAT ACG ACT CCG CAG GCA CC (SEQ ID NO: 21) &5′-CTG-GGA TCC GCT CAG CTT ATT TCA (SEQ ID NO: 22)). PCR reactions wereset up with the following conditions; 94° C. for 5 min., 35× (94° C. for30 s, 48° C. for 30 s, 72° C. for 1 min 30 s) followed by a soak at 72°C. for 5 minutes and a hold at 4° C. The reactions yielded 2 separateoverlapping products and the 2 products were used as the template DNA ina third PCR reaction using the external primers 5′-GGA ATT CCA TAT GCGTCT GTT GAT CGG CT (SEQ ID NO:19) and 5′-CTG-GGA TCC GCT CAG CTT ATT TCA(SEQ ID NO: 22) which incorporated restriction sites for Nde I and BamHI. The reaction conditions were 94° C. for 60 sec followed by 35 cyclesof (30 sec 94° C., 60 sec 49° C., 90 sec 72° C.) followed by 72° C. for5 min. The amplified product was purified with a QiaQuick purificationkit (Qiagen) in accordance with the manufacturer's specifications andthe product was digested with Nde I and BamH I and ligated to pET30avector DNA cut Nde I and BamH I. The ligation products were transformedinto competent cells of E. coli DH5α. The transformants were plated ontoLB plates containing kanamycin (30 μg/ml). Single colonies were screenedby PCR using the primers 5′-TTATGCTAGTTATTGCTCAGCG-3′ (SEQ ID NO:17) and5′-TTCCCCTCTAGAAATAATTTTGT-3′ (SEQ ID NO: 18). PCR products were appliedto an agarose gel and were electrophoretically separated. Colonies whichyielded a product of the correct size (approx. 1 kb) were subsequentlyused to set up overnight cultures, from which miniprep DNA was isolatedusing a QIAGEN Plasmid Purification System according to themanufacturer's protocol. The sequence was confirmed (using primers5′-TTATGCTAGTTATTGCTCAGCG-3′ (SEQ ID NO: 17) and5-TTCCCCTCTAGAAATAATTTTGT-3′ (SEQ ID NO: 18)) and the resultingconstruct was transformed into E. coli HMS174(DE3) competent cells andthe resulting positive transformants were given the name lipB sOspA1/2²⁵¹.

Generation of Constructs without Leader Sequence.

Constructs were prepared with a lipB leader sequence, to which a lipidmoiety is typically attached at the amino terminal cysteine residue.Experimental testing of the recombinant lipidated OspAs verified thepresence of a lipid moiety. However, constructs which did not containthe lipB leader sequence were also prepared. Constructs which did notcontain the lipB leader sequence were made by PCR amplification fromeach of the three lipB constructs (in pET30a) using primers selected togenerate a final product of 769-771 bp without the nucleic acid sequencecoding for the leader sequence and with the codon for the cysteineresidue replaced with a codon for a methionine residue.

PCR reactions comprised 10× buffer [15 mM Tris-HCl (pH 8.0), 50 mM KCl,1.5 mM MgCl2], 200 μm dNTPs, 1.25 U Amplitaq DNA polymerase, 400 nMforward primer 5′-CGTGCGTACCATATGGCACAGAAAGGTGCTGAGTCT-3′ (SEQ ID NO:23) and 400 nM reverse primer 5′-CTGGGATCCGCTCAGCTTATTTCA-3′ (SEQ ID NO:22) and template DNA. PCR conditions were; 94° C. for 5 min, 35× (94° C.for 30 s, 48° C. for 30 s, 72° C. for 1 min 30 s) followed by a soak at72° C. for 5 min and a hold at 4° C. PCR reactions were used directly orstored at ≦□□15° C. until further use.

The PCR products were purified using a QiaQuick PCR purification kit(Qiagen), were digested with Nde I and BamH I and were ligated to pET30avector DNA digested with Nde I and BamH I. The ligation mixes were usedto transform E. coli HMS174(DE3) and colonies containing recombinantplasmids were selected by their resistance to kanamycin and the sequencewas verified from PCR products.

Evaluation of Expression in E. Coli HMS 174(DE3).

Selected colonies were tested for their ability to express therespective novel OspA protein. In each case, single colonies were usedto inoculate LB broth containing kanamycin (30 μg/ml) and were incubatedat 37° C. for 1 to 5 hours until an OD (600 nm) value greater than 0.6and less than 1 was reached. At this point, a sample of the culture wasretained (representing the un-induced sample) and the remainder of theculture was induced by the addition of IPTG to a final concentration of1 mM. The un-induced sample (1 ml) was centrifuged and the pelletretained and stored at −20° C. The induced culture was allowed to growfor a further three hours, after which a 1 ml sample was taken, the OD(600 nm) was measured, the sample centrifuged and the pellet retainedand stored at −20° C.

Preparation of Primary Cells.

Primary cells were prepared for each of the three lipidated constructsand for each of the three non-lipidated constructs. The primary cellscomprised E. coli cells (HMS174(DE3)) carrying a pET30a plasmidexpressing the respective OspA. For preparation of primary cells, asingle colony from the respective stock was picked from a platecontaining kanamycin (30 μg/ml) and rifampicin (200 μg/ml) and was usedto inoculate 500 μl of SMK medium (SOP 8114) and incubated overnight.One hundred microliters of this culture was then used to inoculate 100ml of SMK medium (in duplicate) and the culture was incubated for 17 to20 hours at 37° C. shaking. Sterile glycerol was then added to theculture at a final concentration of 15% and the material was pipetted inaliquots in 500 μl amounts into 60 ampoules, thus yielding 60 ampoulesof primary cells which were directly stored at −80° C.

Three synthetic OspA genes were designed to encode OspA molecules withthe protective epitopes from serotype 1 and 2 OspAs (lipB sOspA 1/2251),serotype 6 and 4 OspAs (lipB sOspA 6/4) and serotype 5 and 3 OspAs (lipBsOspA 5/3). The primary amino acid sequences of these molecules and adescription of the main features incorporated into their design are setout in the following Examples.

Example 3 Description of Lipidated 1/2²⁵¹ OspA (LipB sOspA1/2²⁵¹)

The aim of the study was to design a novel OspA antigen, lipidated1/2²⁵¹ OspA (lipB sOspA 1/2²⁵¹), comprising serotypes 1 and 2. LipBsOspA 1/2²⁵¹, comprises the proximal portion of a serotype 1 OspAsequence (Strain B31, GenBank Accession No. X14407) fused to the distalportion of a serotype 2 sequence (Strain Pko, GenBank Accession No.S48322). The start of the sequence unique to the type 2 serotype is thelysine (K) residue at position 216. The construct was originallydesigned to encode the amino acid alanine (A) at position 251. However,the construct was subsequently altered by PCR to encode an asparagine(N) residue (the actual residue in the published sequence from Pko) toenhance immunogenicity, hence the nomenclature lipB sOspA 1/2²⁵¹.

Secondary features of lipB sOspA 1/2²⁵¹ are shown in the annotated aminoacid sequence of lipB sOspA 1/2²⁵¹ in FIG. 2 and include:

-   -   the replacement of the putative arthritogenic epitope (Gross et        al., 1998), hLFA-1 (YVLEGTLTA) (SEQ ID NO:24), in the proximal        portion of the molecule (amino acids 161 to 185) with an        equivalent sequence (shown in italics and a flanking sequence)        from a serotype 2 OspA sequence (Strain Pko; GenBank Accession        No. S48322): a sequence that is distinct from the hLFA-1        epitope;    -   an OspB leader sequence (amino acids 1 to 15 of FIG. 2) and        various substitutions to avoid prior art. The asparagine (N) and        aspartic acid (D) residues at positions 44 and 46 were replaced        with an aspartic acid (D) and an asparagine (N), respectively,        to produce the sequence KEKDKN (SEQ ID NO: 25). The alanine (A)        and aspartic acid (D) residues at positions 78 and 79 were        replaced with a threonine (T) and an asparagine (N),        respectively, to produce the sequence KTNKSK (SEQ ID NO: 26);    -   stabilizing mutations as described in international patent        publication number WO 02/16421A2 (Luft & Dunn). For example,        methionine (M) replaced arginine (R) at amino acid 136 (R139M);        tyrosine (Y) replaced glutamic acid (E) at amino acid 157        (E160Y); and methionine (M) replaced lysine (K) at amino acid        186 (K189M); and    -   additional stabilizing mutations. For example, threonine (T)        replaced valine (V) at amino acid 173 (aa 176 of the        disclosure). The removal of the putative arthritogenic epitope        (position 161-185), by replacing a B. burgdorferi sequence with        a B. afzelii sequence, disrupted the hydrogen bonding between        amino acids 173 and 174 (aa 176 and 177 of the disclosure). This        led to decreased binding to protective monoclonal antibodies        (105.5 and LA-2 (Jiang et al., J. Immunol. 144: 284-9, 1990;        Golde et al., Infect. Immun. 65: 882-9, 1997; and Ding et        al., J. Mol. Biol. 302: 1153-64, 2000). A threonine (T) was        introduced at position 173, instead of a valine (V), to restore        the hydrogen bond and increase reactivity to protective        monoclonal antibodies 105.5 and LA2.

In addition, amino acids 16-25 (start of the mature protein) areidentical to the OspB sequence (GenBank Accession No. X74810).

The nucleotide and deduced amino acid sequences of lipB sOspA 1/2²⁵¹ areshown in FIG. 3. The leader sequence (green) is cleaved off duringprotein secretion. The sequence of the mature OspA protein starts with acysteine residue (underlined), which forms the attachment site for theprotein's lipid anchor.

Example 4 Description of Lipidated 6/4 OspA (LipB sOspA 6/4)

The aim of the study was to design a novel OspA antigen, lipidated sOspA6/4 OspA (lipB sOspA 6/4), comprising serotypes 4 and 6. LipB sOspA 6/4comprises the proximal portion of a serotype 6 OspA sequence (StrainK48, GenBank Accession No. 140098) fused to the distal portion of aserotype 4 sequence (Strain pTroB; GenBank Accession No. 140089). Thestart of the sequence unique to the type 4 serotype is the asparagine(N) residue at position 217. Secondary features are shown in theannotated amino acid sequence of lipB sOspA 6/4 in FIG. 4 and include:

-   -   stabilizing mutations described in International Patent        Application No. WO 02/16421A2 (Luft and Dunn): methionine (M)        instead of an arginine (R) at amino acid 136, tyrosine (Y)        instead of a glutamic acid (E) at amino acid 157, and        methionine (M) instead of a lysine (K) at amino acid 187; and    -   like lipB sOspA 1/2²⁵¹, described above, an OspB leader sequence        was used (amino acids 1 to 15 in FIG. 4) and amino acids 16-25        are identical to sequence from OspB (GenBank Accession No.        X74810).

Although the peptide sequence KEKNKD (SEQ ID NO: 27) was absent from theparent OspA type 6 sequence (KEKDKD) (SEQ ID NO: 28), the aspartic acid(D) residue at position 46 was replaced with an asparagine residue (N)in conformity with an equivalent change made in the lipB sOspA 1/2²⁵¹construct to produce the sequence KEKDKN (SEQ ID NO:25).

Although the peptide sequence KADKSK (SEQ ID NO:29) was absent from theparent OspA type 6 sequence (KTDKSK) (SEQ ID NO: 30), the aspartic acid(D) residue at position 79 was replaced with an asparagine residue (N)in conformity with an equivalent change made in the lipB sOspA 1/2²⁵¹construct to produce the sequence KTNKSK (SEQ ID NO:26).

Amino acid 37 was changed from the glutaminc acid (E), as present in theparent sequence (Strain K48; GenBank Accession No. 140098), to a valine(V), because almost all type 6 sequences have a valine in this position.

The nucleotide and deduced amino acid sequences of lipB sOspA 6/4 areshown in FIG. 5. The leader sequence (green) is cleaved off duringprotein secretion. The sequence of the mature OspA protein starts with acysteine residue (underlined, see FIG. 5), which forms the attachmentsite for the protein's lipid anchor.

Example 5 Description of Lipidated 5/3 OspA (LipB sOspA 5/3)

The aim of the study was to design a novel OspA antigen, lipidated sOspA5/3 OspA (lipB sOspA 5/3), comprising serotypes 3 and 5. LipB sOspA 5/3comprises the proximal portion of a serotype 5 OspA sequence [DatabaseAccession No. emb|X85441|BGWABOSPA, B. garinii OspA gene (WABSousubstrain)] fused to the distal portion of a serotype 3 sequence (StrainPBr; Genbank Accession No. X80256, B. garinii OspA gene) withmodifications as shown in SEQ ID NOS: 5 and 6. The start of the sequenceunique to the type 3 serotype is the aspartic acid (D) residue atposition 216. Secondary features are shown in the annotated amino acidsequence of lipB sOspA 5/3 in FIG. 6 and include:

-   -   stabilizing mutations described in International Patent        Application No. WO 02/16421A2 (Luft and Dunn): methionine (M)        instead of an arginine (R) at amino acid 136; tyrosine (Y)        instead of a glutamic acid (E) at amino acid 157; and        methionine (M) instead of a lysine (K) at amino acid 187; and    -   like lipB sOspA 1/2²⁵¹ and lipB sOspA 6/4, described above, an        OspB leader sequence was used (amino acids 1 to 15 in FIG. 6)        and amino acids 16-25 are identical to sequence from OspB        (GenBank Accession No. X74810).

Although the peptide sequence KEKNKD (SEQ ID NO:27) was absent from theparent OspA type 5 sequence (KEKDKD) (SEQ ID NO: 28), the aspartic acid(D) residue at position 46 was replaced with an asparagine residue (N)in conformity with an equivalent change made in the lipB sOspA 1/2²⁵¹construct giving the sequence KEKDKN (SEQ ID NO:25).

Although the peptide sequence KADKSK (SEQ ID NO:29) was absent from theparent OspA type 5 sequence (KTDKSK) (SEQ ID NO: 30), the aspartic acid(D) residue at position 79 was replaced with an asparagine residue (N)in conformity with an equivalent change made in the lipB sOspA 1/2251construct giving the sequence KTNKSK (SEQ ID NO: 26).

The nucleotide and deduced amino acid sequences of lipB sOspA 5/3 areshown in FIG. 7. The leader sequence (green) is cleaved off duringprotein secretion. The sequence of the mature OspA protein starts with acysteine codon (underlined, see FIG. 7), which forms the attachment sitefor the protein's lipid anchor.

Example 6 Optimization of Codon Usage for High Level Expression in E.Coli

Because the presence of codons that are rarely used in E. coli is knownto present a potential impediment to high-level expression of foreigngenes, low-usage codons were replaced with codons which are used byhighly expressed genes in E. coli. The nucleotide sequences of the novelOspA genes were designed to utilize the codons found most frequently(preferred codons) among the highly expressed class II, E. coli genes(Guerdoux-Jamet et. al., DNA Research 4:257-65, 1997). The data forcodon usage among the novel OspA genes and for the highly expressedclass II E. coli genes are summarized in Tables 7 and 8. The data forthe less frequent amino acids for which tRNA molecules are less likelyto be rate limiting is presented separately (Table 7) from the data forthe amino acids which occur most often (Table 8).

TABLE 7 Codon usage in novel OspA genes (less common amino acids*) AminoOspA 1/2 AA Counts OspA 5/3 AA Counts OspA 6/4 AA Counts Class II AcidCodon Total Codon % Total Codon % Total Codon % Counts (%) Gln CAA 5 120.0 4 0 0.0 4 0 0.0 18.7 CAG 4 80.0 4 100.0 4 100.0 81.4 Phe TTT 5 120.0 6 3 50.0 6 1 16.7 29.1 TTC 4 80.0 3 50.0 5 83.3 70.9 Met ATG 4 4100.0 5 5 100.0 4 4 100.0 100.0 Tyr TAT 4 1 25.0 4 1 25.0 4 0 0.0 35.2TAC 3 75.0 3 75.0 4 100.0 64.8 Arg CGT 2 2 100.0 3 3 100.0 2 2 100.064.3 CGC 0 0.0 0 0.0 0 0.0 33.0 CGA 0 0.0 0 0.0 0 0.0 1.1 CGG 0 0.0 00.0 0 0.0 0.8 AGA 0 0.0 0 0.0 0 0.0 0.6 AGG 0 0.0 0 0.0 0 0.0 0.3 CysTGT 1 0 0.0 1 1 100.0 1 0 0.0 38.9 TGC 1 100.0 0 0.0 1 100.0 61.2 ProCCT 1 0 0.0 2 0 0.0 1 0 0.0 11.2 CCC 1 100.0 1 50.0 1 100.0 1.6 CCA 00.0 0 0.0 0 0.0 15.3 CCG 0 0.0 1 50.0 0 0.0 71.9 Trp TGG 1 1 100.0 1 1100.0 1 1 100.0 100.0 *i.e. Amino acids that, individually, make up<2.5% of the total amino acids by number.

TABLE 8 Codon usage in novel OspA genes (more prevalent amino acids)Amino OspA 1/2 AA Counts OspA 5/3 AA Counts OspA 6/4 A A Counts Class IIAcid Codon Total Codon % Total Codon % Total Codon % Counts (%) Lys AAA40 30 75.0 40 36 90.0 40 37 92.5 78.6 AAG 10 25.0 4 10.0 3 7.5 21.5 ThrACT 32 13 40.6 31 15 48.4 34 7 20.6 29.1 ACC 14 43.8 16 51.6 27 79.453.6 ACA 0 0.0 0 0.0 0 0.0 4.7 ACG 5 15.6 0 0.0 0 0.0 12.7 Leu CTT 27 311.1 28 2 7.1 28 1 3.6 5.6 CTC 3 11.1 0 0.0 4 14.3 8.0 CTA 0 0.0 0 0.0 00.0 0.8 CTG 17 63.0 21 75.0 18 64.3 76.7 TTA 2 7.4 2 7.1 3 10.7 3.4 TTG2 7.4 3 10.7 2 7.1 5.5 Ser TCT 25 9 36.0 25 12 48.0 23 8 34.8 32.4 TCC 832.0 3 12.0 8 34.8 26.6 TCA 0 0.0 0 0.0 0 0.0 4.8 TCG 0 0.0 0 0.0 0 0.07.4 AGT 0 0.0 0 0.0 0 0.0 4.5 AGC 8 32.0 10 40.0 7 30.4 24.3 Gly GGT 2211 50.0 23 8 34.8 22 9 40.9 50.8 GGC 11 50.0 14 60.9 13 59.1 42.8 GGA 00.0 0 0.0 0 0.0 2.0 GGG 0 0.0 1 4.3 0 0.0 4.4 Val GTT 22 8 36.4 15 640.0 18 7 38.9 39.8 GTC 4 18.2 0 0.0 4 22.2 13.5 GTA 3 13.6 9 60.0 316.7 20.0 GTG 7 31.8 0 0.0 4 22.2 26.8 Glu GAA 21 16 72.7 22 18 81.8 2118 85.7 75.4 GAG 5 23.8 4 18.2 3 14.3 24.7 Asp GAT 17 8 47.1 16 9 56.319 8 42.1 46.1 GAC 9 52.9 7 43.8 11 57.9 54.0 Ala GCT 16 6 37.5 18 950.0 17 6 35.3 27.5 GCC 0 0.0 1 5.6 4 23.5 16.1 GCA 5 31.3 6 33.3 3 17.624.0 GCG 5 31.3 2 11.1 4 23.5 32.3 Asn AAT 13 3 23.1 13 3 23.1 13 2 15.417.3 AAC 10 76.9 10 76.9 11 84.6 82.8 Ile ATT 12 4 33.3 13 5 38.5 13 323.1 33.5 ATC 8 66.7 8 61.5 10 76.9 65.9 ATA 0 0.0 0 0.0 0 0.0 0.6

The high degree of concordance between codon usage chosen for the novelOspA genes (common amino acids only) and among E. coli class II genes isapparent (i.e. plot of percentage figures from Table 8 for class IIgenes against individual novel OspA genes; see FIG. 8). For the threelipidated constructs, the original sequences had a GC content rangingfrom 32.8% to 33.8%, while the codon-optimized sequences had a GCcontent ranging from 43.8% to 46.8%, which is similar to the 50% GCcontent of E. coli.

Example 7 Construction of Synthetic Non-Lipidated OspA Genes

Constructs were also prepared which did not contain the lipB leadersequence. The two sets of constructs (lipidated and non-lipidated) areneeded to evaluate their ease of production in the fermentor (biomass,stability, product yield, and the like), to assess how readily thedifferent types of antigen can be purified and to compare theirbiological characteristics (safety profile and protective potency).

The constructs (SEQ ID NOS: 7, 9, and 11) were generated by PCRamplification from each of the three lipB OspA constructs (SEQ ID NOS:1, 3, and 5) using PCR primers with incorporated restriction sites. ThePCR products were purified, digested with Nde I and BamH I and ligatedto digested pET30a vector DNA. The ligation mixes were used to transformE. coli DH5α□ and the OspA sequences were verified. Miniprep DNA wasprepared, isolated, and used to transform HMS 174(DE3) host cells. Thesequences of the non-lipidated derivatives are identical to thelipidated versions, except they lack the first 45 base pairs coding forthe leader sequence and contain an Nde I site which contains amethionine codon which replaces the cysteine codon in the lipidatedversions (see FIG. 9).

Example 8 Expression of Novel Recombinant OspA Antigens

To express/produce the novel recombinant OspA genes for antigenicpurposes, an E. coli expression system controlled by the bacteriophageT7 RNA polymerase (Studier et al., J. Mol. Biol. 189:113-30, 1986) wasused. In this expression system, the novel OspA genes were cloned intothe multiple cloning site in one of the pET series of plasmids (e.g.,pET30a). Because expression of the foreign gene is under the control ofa bacteriophage T7 promoter, which is not recognized by E. coli RNApolymerase, expression is dependent on a source of T7 RNA polymerase.This enzyme is provided when the recombinant plasmids are transferredinto an appropriate expression host, such as E. coli HMS174(DE3), whichcontains a chromosomal copy of the T7 RNA polymerase gene. Expression ofthe chromosomally integrated T7 RNA polymerase gene is under control ofa lacUV5 promoter, which can be switched on (i.e. induced) by theaddition of isopropyl β-D-1-thiogalactopyranoside (IPTG) or lactose (seeFIG. 10). Consequently, expression of the foreign gene is also regulatedby the addition of the inducer molecule.

The cells were induced at late log-phase and harvested 3-4 hours afterinduction. In induced cells, the chimeric OspA antigen was the mosthighly expressed protein as determined by SDS-PAGE of cell lysates. Mostof the OspA chimeras were found in the supernatant. Contaminating E.coli proteins were removed by anion-exchange chromatography and thechimeric OspA proteins eluted in the void volume were concentrated byultrafiltration.

The expression of the novel recombinant OspA proteins from each of theconstructs was tested, and samples from induced and un-induced cultureswere run on an SDS polyacrylamide gel (FIG. 11). For the lipidated (SEQID NOS: 2, 4, and 6) and non-lipidated (SEQ ID NOS: 8, 10, and 12)antigens, a band of approximately 31 kDa was observed in each case (seeFIG. 11). The proteins were characterized and the molecular weightsdetermined correlated (+/−0.5 daltons) with the theoretical molecularweights assuming the terminal methionine is cleaved off. FIG. 11 showsthat the expressed recombinant lipidated OspA proteins comprise at least10% of the total protein yield, verifying that the constructs are usefulfor their intended purpose.

Example 9 A Single Recombinant OspA Antigen (R OspA 1/2) ProtectsAgainst Infection with B. Burgdorferi s.s. and B. afzelii

The purpose of this study was to determine if a single recombinantantigen (rOspA 1/2; the polypeptide comprising SEQ ID NO: 2 (lipB sOspA1/2²⁵¹)), designed to retain the protective properties of OspA serotypes1 and 2, is able to induce antibody responses which protect mice againstinfection with either B. burgdorferi s.s. (OspA serotype 1) or B.afzelii (OspA serotype 2). Evidence is provided to show that theinclusion of additional rOspA antigens did not have an antagonisticeffect on the protective immunity afforded by the rOspA 1/2 antigen.

Design and Construction of rOspA 1/2.

To eliminate the risk of introducing adventitious agents, complementaryoverlapping synthetic oligonucleotides were used to generate DNAfragments that were ligated together and cloned into vector pET30a andthe sequence was verified. This approach also enabled codon usage to beoptimized for the E. coli host HMS174 (DE3) used to express the OspAgene. The novel gene is based on the proximal portion of a serotype-1OspA sequence (amino acids 29 to 218, Strain B31; GenBank AccessionNumber X14407) fused to the distal portion of a serotype-2 sequence(amino acids 219 to 273, Strain PKo; Accession Number S48322). The 25amino acid fragment from B. burgdorferi strain B31 (aa 164 to 188) wasreplaced with sequence from B. afzelii strain PKo (aa 164 to 188)because this region of the B31 OspA (aa 165-173) is highly related tothe region encompassing the hLFA-1 epitope (aa 332-340). The N-terminalsequence including the leader sequence and the first 11 amino acids werederived from OspB (Strain B31; GenBank Accession Number X74810) in orderto optimize lipidated protein expression. Other specific amino acidchanges were made to improve the immunogenicity and conformationalstability of the rOspA 1/2 molecule and the sequence of rOspA 1/2 (lipBsOspA 1/2²⁵¹) is set out in SEQ ID NO: 2.

Animal Testing.

The ability of a single recombinant OspA antigen (rOspA 1/2) to preventinfection with two species of Borrelia, which express different OspAantigens, was assessed in C3H/HeJ mice immunized subcutaneously (days 0and 28) with purified OspA antigen (0.1 μg or 0.03 μg doses) formulatedwith 0.2% (w/v) aluminum hydroxide as adjuvant. Mice were challenged 2weeks after the booster immunization, either by intradermal injection(needle challenge; 7×10⁴ cells) or by the natural route of infection(tick challenge). For the latter experiments, 8 nymphal ticks wereapplied per mouse and allowed to feed for up to 5 days. The nymphs werecollected in the vicinity of Budweis (Czech Republic), an area endemicfor Lyme disease. The majority of these ticks were infected with B.afzelii as determined by testing unfed ticks by PCR. The infectiousstatus of the mice was determined four weeks later. In the tickchallenge experiments, the presence of Borrelia was confirmed by culture(urinary bladder) and by detection of Borrelia DNA by real-time PCR(heart). Animal experiments were conducted in accordance with Austrianlaws on animal experimentation and international guidelines (AAALAC andOLAW) and were reviewed by the Institutional Animal Care and UseCommittee and approved by the Austrian regulatory authorities.Immunogenicity. The antibody response (μg IgG/ml) to rOspA 1/2 antigenwas determined by ELISA using rOspA 1/2 as the coating antigen and anOspA specific monoclonal antibody (prepared in house) with a defined IgGcontent as a standard.

Diagnostic Procedures.

For the needle challenge experiments, the presence of antibodies to aconserved epitope in the surface-exposed lipoprotein VIsE protein (C6ELISA; coated plates from Immunetics® C6 Lyme ELISA™) or to Borreliaantigens other than the OspA immunogen (Western blotting) was used todiagnose infection. Western blotting used a cell lysate prepared from B.burgdorferi s.s. strain ZS7 as this was the challenge organism. Animalswere deemed infected if they were positive in both assays.

For the tick challenge experiments, the C6 ELISA and Western blottingwere also done. However, Western blotting used lysates from B.burgdorferi s.s. ZS7, B. afzelii ACA1 and B. garinii KL11, because theidentity of the infecting organism was unknown. Animals were consideredto have undergone seroconversion only if both assays were positive. Inaddition, Borrelia infection was assessed by culture from the urinarybladder and by detection of B. burgdorferi s.l. nucleic acids in genomicDNA extracted from heart tissue using a real-time PCR assay targetingthe 5′-region of OspA and a 16S rRNA gene-based assay. Animals werescored as PCR-positive only if a PCR product was detected with bothassays. Overall, to judge an animal as infected, mice needed to bepositive either by culture, PCR or serology.

Characterization of Infecting Borrelia.

Where possible, the infecting organism was cultured and the OspAsequence and deduced amino acid sequence determined for OspA residues38-262 (B. afzelii VS461, GenBank Accession Number Z29087). Thisinformation was compared to OspA reference sequences so that the OspAtype and Borrelia species could be inferred. For species which express asingle OspA serotype, the OspA sequence for the type strain for thespecies was chosen as a reference, e.g., B. afzelii VS461 or B.valaisiana VS116 (GenBank Accession Number Z29087; AF095940). As B.garinii has multiple OspA types, OspA sequences for OspA genotypes 3-7were used (i.e. strains PBr, PTrob, WABSou, Tlsl and T25; GenBankAccession Numbers X80256, X80186, X85441, X85440 and X80254,respectively). For real-time PCR-based typing, sequence alignments ofthe OspA gene of 124 B. burgdorferi s.l. species deposited in GenBankwere inspected for serotype-specific sequences and suitable primer-probecombinations were designed using Primer Express 3.0 (AppliedBiosystems). All assays were run on an ABI Prism® 7900HT sequencedetection unit using universal cycling conditions.

Prevention of B. Burgdorferi s.s (OspA Serotype-1) Infection byImmunization with rOspA 1/2.

All of the mice immunized with low doses of two different lots of therOspA 1/2 antigen developed IgG antibodies specific for the immunogen asdetermined by ELISA. No antibodies were detected in the control micewhich had been treated with vaccine formulation buffer containingaluminum hydroxide. To assess the ability of this immune response toprevent infection with B. burgdorferi s.s., a species that encodes aserotype-1 OspA, the mice were injected intradermally with 7×10⁴ cellsof B. burgdorferi s.s. strain ZS7. All of the control mice treated withbuffer containing adjuvant showed serological evidence of infection asdemonstrated by C6 ELISA and by Western blotting. None of the miceimmunized with the rOspA 1/2 antigen became infected and the sera fromthese mice were negative by both assays. As little as 0.03 μg of therOspA 1/2 antigen, when formulated with aluminum hydroxide as adjuvantand administered in a two dose immunization regimen, conferred 100%protection (P<0.0001, Fisher exact two tailed test) against a needlechallenge with the virulent B. burgdorferi s.s. strain ZS7.

Prevention of B. afzelii (OspA Serotype-2) Infection by Immunizationwith rOspA 1/2.

To assess the ability of immunization with the rOspA 1/2 antigen toprevent infection with B. afzelii, a species that encodes a serotype-2OspA, mice were immunized, in two separate experiments, with the sameantigen lots and study design as used in the needle challenge experimentdescribed above. However, in this case, the immunized mice werechallenged with feral ticks (nymphs) known to be infected mainly with B.afzelii. The ability of these feral ticks to transmit B. burgdorferis.l. to mice was confirmed by challenging non-immunized control animals.

Most of the control mice (total 11/14, 79%) became infected. Allinfected control animals were positive for Borrelia DNA by twoindependent real-time PCR assays (16S rRNA and OspA genes). In 10/11cases, it was possible to isolate Borrelia by culture of the urinarybladder. The remaining mouse was positive by serology and PCR. For 9 ofthe 10 culture isolates, OspA sequences were retrieved and all weretyped as B. afzelii (>99% OspA sequence identity). Furthermore, allinfecting organisms were typed as B. afzelii by PCR analysis of the DNAextracted from the heart using a real-time PCR assay specificallytargeting serotype 2 OspA genes. These data confirm that B. afzelii wasthe principal Borrelia species being transmitted from the infected feralticks to their mouse host.

Few of the mice immunized with rOspA 1/2 (total 3/32, 9%) becameinfected. Of these three mice, one was infected as determined by allthree diagnostic criteria (serology, PCR and culture) and sequenceanalysis revealed that the infecting organism was B. garinii serotype-6(>99% OspA sequence identity). The remaining two animals deemed infectedwere positive by only two of the three criteria. One mouse was positiveby serology and PCR. However, the infecting organism could not beretrieved in culture. Nevertheless, this organism could be typed as B.garinii serotype-7 by PCR analysis of the DNA extracted from the heartusing PCR specific for the serotype-7 OspA gene. The third mouse was PCRand culture positive but serologically negative. The isolate culturedfrom this mouse was B. valaisiana as determined by sequencing (OspAsequence identity with B. valaisiana strain VS116). Importantly, none ofthe immunized mice (0/32) became infected with B. afzelii. As little as0.03 μg of the rOspA 1/2 antigen, when formulated with aluminumhydroxide as adjuvant and administered in a two dose immunizationregimen, conferred full protection against B. afzelii transmitted byferal ticks.

Conclusion.

A single recombinant outer surface protein A (OspA) antigen designed tocontain protective elements from two different OspA serotypes (1 and 2)was able to induce antibody responses which protect mice againstinfection with either B. burgdorferi sensu stricto (OspA serotype-1) orB. afzelii (OspA serotype-2). Protection against infection with B.burgdorferi s.s. strain ZS7 was demonstrated in a needle challengemodel. Protection against B. afzelii species was shown in a tickchallenge model using feral ticks. In both models, as little as 0.03 μgof antigen, when administered in a two dose immunization schedule withaluminum hydroxide as adjuvant, was sufficient to provide completeprotection against the species targeted. As anticipated, the protectionafforded by this novel antigen did not extend to other Borrelia speciesas demonstrated by the antigen's inability to provide protection againstinfection with B. garinii and B. valaisiana strains. This proof ofprinciple study proves that knowledge of protective epitopes can be usedfor the rational design of effective, genetically-modified vaccinesrequiring fewer OspA antigens and suggests that this approach mayfacilitate the development of an OspA vaccine for global use.

Example 10 Efficiency of Mouse Anti-OspA Antibodies to Bind to theSurface of Live Borrelia or to Inhibit Growth Thereof Correlates withProtection Against Needle Challenge Using a B. Burgdorferi s.s. Type 1Strain

The purpose of this study was to establish correlates of protection formice immunized with the rOspA 1/2 antigen in a needle challenge modelusing a Borrelia burgdorferi sensu stricto OspA type 1 strain.Parameters analyzed were the potency of anti-OspA antibodies to bind tothe surface of live Borreliae or to inhibit growth of Borreliae.

98 mice were deliberately immunized with a sub-optimal 3 ng dose of therOspA 1/2 antigen adjuvanted with 0.2% Al(OH)3), which was 10-fold lowerthan the lower dose used in Example 9, in a prime-booster regimen sothat, upon challenge, both protected and infected animals would beobserved. Vaccination was carried out subcutaneously using a dose volumeof 100 μl on days 0, 14 and 28. On day 38, pre-challenge sera sampleswere taken from 96 mice, and animals were challenged 10 days later with19.4×ID₅₀ of culture grown B. burgdorferi s.s. ZS7, and infection statuswas determined after four weeks. 71 of the 96 mice (72%) were found tobe protected after immunizing with this low dose of antigen.

Four weeks post-challenge blood was taken to identify infected mice byWestern blotting their sera against a membrane fraction of B.burgdorferi s.s. strain ZS7. At the challenge doses used, only infectedmice had an antibody response to membrane antigens of strain ZS7 otherthan OspA (the response to OspA, induced by vaccine, was not scored).

Quantitation of OspA Antibody Binding to the Surface of Live Borreliae.

In this assay, B. burgdorferi s.s. strain B31 expressing OspA types 1were incubated at a fixed dilution (1:100) with the pre-challenge mousesera at room temperature in the presence of EDTA to prevent complementactivation. After washing to remove unbound antibody, antibodies thatwere specifically bound to the cell surface were labeled by incubatingthe treated cells with an r-Phycoerythrin-conjugated anti-mouse Igpolyclonal antibody. Subsequently, a DNA stain (LDS-751) that emits redfluorescence, thereby enhancing detection, was used, and bacteria werethen analyzed by flow cytometry (FACSCalibur, Beckton-Dickinson). Thefluorescence intensity, which correlates with the number of antibodymolecules attached to the cell surface, was recorded for at least 2,000individual Borreliae, and the mean of the fluorescence intensities (MFI)was calculated. Normal mouse serum served as the negative control toevaluate the extent of non-specific surface binding of antibodies, whilean OspA serotype 1-specific mAb served as a positive control to confirmthe identity of the OspA type and to verify the level of OspA expressionof the cells in the bacterial culture.

A Bacterial Growth Inhibition Assay.

To measure the potency of the pre-challenge sera to inhibit growth ofthe Borreliae, B. burgdorferi s.s. strain B31 expressing OspA type 1 wascultured at 33° C. in the presence of serial dilutions ofheat-inactivated pre-challenge or non-immune mouse serum (negativecontrol) in the presence of complement (normal guinea pig serum). Whenthe bacteria in the control cultures incubated with non-immune sera hadgrown sufficiently, as determined microscopically, accurate cell countswere made by flow cytometric analysis. Cell cultures were mixed with asolution containing a defined number of fluorescence-labeled beads and aDNA-dye was added to fluorescently label the Borrelia cells. Sampleswere processed using a FACSCalibur Flow cytometer until 100 beads werecounted, and the absolute cell concentrations were calculated (cells/ml)by comparing the numbers of events in the gate defining the beads and inthe gate defining the Borreliae. The serum dilution that inhibitedbacterial growth by 50% was calculated in comparison to the NMS controland reported as GI-50 titer. A standard serum preparation was used tonormalize titers between different assays. Distribution of the measuredserum parameters were compared among infected and protected animals bythe non-parametric Mann-Whitney U test (Graphpad Prism Vers. 5.0).

Results of this study (see FIG. 19) clearly demonstrate that a highlysignificant correlation exists between the functional antibody contentof the immune serum at the time of challenge and protection againstinfection with a high dose (19.4×ID₅₀) needle challenge of B.burgdorferi s.s. (ZS7). FACS-based fluorescence intensity measurementsof live Borreliae expressing OspA type 1, which reflects the number ofanti-OspA antibody molecules attached to the cell surface, carried outafter incubation of the bacteria with the pre-challenge sera at a fixeddilution, correlated best with protection (p<0.0001 Mann-Whitney Utest). However, growth inhibition titers also correlated highlysignificantly with protection (p=0.0002 Mann-Whitney U test, FIG. 19).

Example 11 Efficiency of Mouse Anti-OspA Antibodies to Bind to theSurface of Live Borrelia or to Inhibit Growth Correlates with ProtectionAgainst Tick Challenge Using a B. afzelii Type 2 Strain

The purpose of this study was to establish correlates of protection ofmice immunized with the chimeric OspA 1/2 antigen in a tick challengemodel, which utilizes the natural infection route by using feral tickscollected from Budweis in the Czech Republic to infect the mice. Sincenymphal ticks from this endemic area are so predominantly infected withB. afzelii, they are considered to provide a B. afzelii OspA type 2strain challenge. As set out in Example 10, the parameters analyzed werethe potency of anti-OspA antibodies to bind to the surface of liveBorreliae or to inhibit growth of Borreliae, both of which had beenshown to correlate well against needle challenge with Borreliabugdorferi s.s. Thus, this study serves to extend the applicability ofusing these two parameters as correlates of protection against naturalinfection of B. afzelii, the most prominent human disease associatedgenospecies in Europe.

Forty mice were immunized with a sub-optimal 3 ng dose of the rOspA 1/2antigen adjuvanted with 0.2% Al(OH)3), which was 10-fold lower than thelower dose used in Example 9, in a prime-booster regimen. As in Example10, this sub-optimal dose was chosen in order to ensure that bothprotected and infected animals would be observed after challenge.Vaccination was carried out subcutaneously using an injection volume of100 μl on days 0, 14 and 28. On day 40, individual blood samples weretaken from the mice to generate pre-challenge sera. Because the limitednumber of ticks available did not allow the challenge of all 40 mice, 20mice were selected based on surface binding and anti-type 2 IgGconcentrations to cover a broad range of responses. Eight ticks wereapplied to each mouse and were allowed to feed on the mice for 5 days.Four weeks after the challenge, the mice were sacrificed and theinfectious status of the immunized and control mice was determined byWestern blotting of sera against membrane antigens from B. burgdorferis.s., B. afzelii and B. garinii; culture of Borrelia organisms from thebladder; and real time PCR detection of Borrelia from DNA extracted fromthe bladder.

Quantitation of OspA Antibody Binding to the Surface of Live Borreliae.

In this assay, B. afzelii strain Arcon expressing OspA type 2 wasincubated at a fixed dilution (1:100) with the pre-challenge mouse seraat room temperature in the presence of EDTA to prevent complementactivation. After washing to remove unbound antibody, antibodiesspecifically bound to the cell surface were labeled by incubating thetreated cells with an r-Phycoerythrin-conjugated anti-mouse Igpolyclonal antibody. All subsequent steps in the assay where similar tothose described in Example 10. Normal mouse serum served as the negativecontrol for non-specific antibody binding. A high titer mouse serumraised against the tri-component rOspA vaccine formulation, togetherwith OspA serotype 2-specific mAbs served as positive controls toconfirm OspA serotype specificity and the OspA expression level of cellsin the bacterial culture.

Bacterial Growth Inhibition Assay.

To measure the potency of the pre-challenge sera to inhibit growth ofBorreliae, the B. afzelii strain Arcon expressing OspA type 2 wascultured at 33° C. in the presence of serial dilutions ofheat-inactivated pre-challenge or non-immune mouse serum (negativecontrol) without complement. When the bacteria in the control cultures,which were incubated with non-immune sera, had grown sufficiently, asdetermined microscopically, accurate cell counts were made by flowcytometric analysis. The procedure used to count the bacteria wassimilar to that previously described for the growth inhibition assay inExample 10. The serum dilution which inhibited bacterial growth by 50%was calculated in comparison to the NMS control and reported as GI-50titer. A standard serum preparation was used to normalize titers betweendifferent assays.

Statistical Analysis.

Distribution of the measured serum parameters were compared in infectedand protected animals by the non-parametric Mann-Whitney U test(Graphpad Prism Version 5.0).

Results.

Of the 20 animals immunized three times with 0.003 pg of rOspA 1/2 andchallenged with 8 feral ticks, 7/20 (35%) were found to be infected. Dueto limited tick availability, it was not possible to determine the exactinfection rate of the challenge by challenging a control group ofnon-immunized mice. However, this challenge was not required for thepurpose of the present study, and typically a rate of infection of70-80% is achieved in challenge experiments with feral ticks fromBudweis.

Significant differences were detected between the protected and infectedgroups for the results of the surface binding (p=0.007) and growthinhibition (p=0.03) assays (FIG. 20).

Conclusion.

In this study it has been shown that a statistically significantcorrelation exists between the functional antibody content in mouseserum at the time of challenge and the protection against infection witha feral tick challenge applying 8 ticks per mouse. FACS-basedfluorescence intensity measurements of live Borreliae expressing OspAtype 2, which reflects the number of anti-OspA antibody moleculesattached to the cell surface performed after incubation of the bacteriawith the pre-challenge sera at a fixed dilution, correlated best withprotection. Growth inhibition titers also correlated well withprotection. In contrast to Borrelia burgdorferi s.s. strains, wherecomplement is required for efficient killing, rOspA1/2 antigen inducedantibodies that effectively inhibit Borrelia growth even in the absenceof complement.

The results of the studies presented in Example 10 and 11, when takentogether, establish the in vitro parameters of the mean fluorescentintensity (MFI) of surface bound antibody to live Borreliae and theGI-50 titer of immune mouse sera as “correlates of protection” in bothexamples where active mouse protection models are currently available(e.g., namely, a needle challenge model for B. burgdorferi s.s. OspAType 1 strains and a tick challenge model for B. afzelii OspA Type 2strains. Moreover, in the absence of reliable active protection modelsfor evaluating protection against homologous B. garinii strainsexpressing OspA types 3-6, by inference, the aforementioned models canbe used as in vitro “surrogate markers of protection” to evaluate theprotective potential and cross strain coverage of various vaccineformulations for strains expressing all the vaccine homologous OspAtypes and even for those expressing heterologous OspA types. Indeed,when studies using these functional immune response assays were carriedout on immune sera from mice immunized with the 3-component chimericrOspA vaccine formulation, then comparable MFI and GI-50 titers wereobtained for B. garinii (OspA types 3, 4, 5, 6) (see Examples 13), thusindicating, through these surrogate markers of protection, thatprotective responses were also achieved against strains for whichcurrently no active mouse protection model exists. Furthermore, bycomparing the immune responses of mice immunized with either (a),individual chimeric rOspA antigens; (b), or any one of the possible2-component chimeric rOspA antigen vaccine formulation combinations; or(c), the 3-component chimeric rOspA antigen formulation, it was possibleto show that the latter 3-component vaccine was required to optimallycover strains expressing OspA types 1-6 (Example 14). Moreover, throughthe use of these in vitro surrogate marker assays, it was possible toshow that immune responses produced after immunizing mice with the3-component chimeric rOspA vaccine formulation (rOspA 1/2, rOspA 6/4 andrOspA 5/3) do induce functional immune responses to all intra typevariants (or subtypes) of types 1, 2, 3, 5, and 6 tested to date (seeExample 15) and even to heterologous OspA types, other than thehomologous OspA types 1-6 present within the vaccine (see Example 16).

Example 12 Multivalent Recombinant OspA Formulation Comprising 3Antigens (1/2, 6/4, and 5/3) is Highly Immunogenic in Mice

A multivalent OspA vaccine (rOspA 1/2, rOspA 5/3, and rOspA 6/4) wasevaluated in a tick challenge model. Three recombinant OspA antigenscontaining the protective epitopes from OspA serotype 1 and 2 (SEQ IDNO: 2), OspA serotype 6 and 4 (SEQ ID NO: 4), and OspA serotype 5 and 3(SEQ ID NO: 6) were combined in a vaccine.

Groups of ten female C3H/HeJ mice (age at immunization: 11 weeks) wereimmunized subcutaneously on days 0 and 28 with a fixed dose of 0.3 μg ofthe multivalent vaccine (0.1 μg of each, rOspA 1/2, rOspA 5/3, and rOspA6/4). The tick challenge was done as described herein above with ticksfrom Budweis, Czech Republic. The ability of the feral ticks to transmitB. burgdorferi s.l. to mice was confirmed by challenging un-immunizedcontrol animals. The infection status of the challenged mice wasdetermined by Western blotting, real-time PCR, and by culture.

Interim blood samples were taken on day 41 by orbital puncture. Finalblood samples (day 70/71) were collected by heart puncture. Individualsera were prepared from whole blood by centrifugation (10 minutes;1000-2000×G; RT). Sera were stored at ≦−20° C. until use.

In this experiment unfed ticks, taken from the same batch used tochallenge the mice, were characterized to determine the overallinfection rate and to confirm the species of the infecting organisms.When 80 nymphal ticks were tested for the presence of B. burgdorferis.l. DNA by 16S rRNA real-time PCR, 32.5% (26/80) were found to beinfected. The OspA-serotype could be determined by PCR-ELISA for 22 ofthe 26 infected nymphs; 86% (19/22) were typed as B. afzelii and 14%(3/22) as B. burgdorferi s.s.

All of the non-immunized control mice (100%; 10/10) became infected,whereas only one of the mice immunized with the multivalent rOspAvaccine became infected (10%; 1/10). There was 100% agreement betweenthe different methods used to identify infected mice. The multivalentrOspA vaccine resulted in a statistically highly significant protection(p=0.00012; Fisher's exact two tailed test) when compared to the controlgroup.

These data show that immunization with a multivalent rOspA vaccine,which contains the rOspA 1/2 antigen, is able to prevent infection withB. afzelii, a Borrelia species which expresses a serotype 2 OspA.Further, there is no evidence that the inclusion of additional rOspAantigens has an antagonistic effect on the protective immunity affordedby the rOspA 1/2 antigen.

This vaccine provided protection against tick-transmitted infection withB. afzelii which was equivalent to that seen with the OspA 1/2 antigen;0.3 μg of the vaccine (0.1 μg of each antigen) formulated with 0.2%Al(OH)3 and administered in a two dose schedule provided 90% protectionas determined by Western blot, culture of Borrelia and detection ofBorrelia DNA by PCR.

Example 13 A Vaccine Comprising the Three-Component Vaccine (OspA 1/2,OspA 6/4, and OspA 5/3) Induces High Levels of Functional Anti-OspAAntibodies which Bind to and Inhibit Growth of Borrelia StrainsExpressing OspA Types 1-6

Since both surface binding (MFI) and growth inhibition (GI-50 titers)were shown to be good correlates of protection in a needle challenge (B.burgdorferi s.s.) model (Example 10) and in a tick challenge (B.afzelii) mouse model (Example 11), the present study was undertaken todetermine if equivalent functional immune responses are induced by the3-component chimeric rOspA antigen vaccine formulation against B.garinii OspA serotypes 3-6, for which no in vivo protection model isavailable to investigate the efficacy of a vaccine.

Mouse Immunization.

Groups of 10 female C3H/HeJ mice were immunized subcutaneously threetimes (day 0, day 14, day 28) with a 1:1:1 mixture of rOspA-1/2,rOspA-6/4 and rOspA-5/3) at three different doses (1, 0.1, 0.03 μgprotein per dose) combined with 0.2% Al(OH)3 as an adjuvant. Serum wasgenerated from blood samples taken on day 40.

Quantitation of OspA antibody binding to the surface of live Borreliae.In this assay, in vitro grown cultures of six representative Borreliastrains expressing OspA types 1-6 (B. burgdorferi sensu strictoB31/OspA-1; B. afzelii Arcon/OspA-2; B. garinii PBr/OspA-3; B. gariniiDK6/OspA-4; B. garinii W/OspA-5; and B. garinii KL11/OspA-6) wereincubated at a fixed dilution (1:100) with pools of the peak titer mousesera at room temperature in the presence of EDTA to prevent complementactivation. The subsequent washing, labeling, detection and analysisprocedures were similar to those described in Example 10. Normal mouseserum served as the negative control for non-specific binding ofantibodies.

Bacterial Growth Inhibition Assay.

To measure the potency of the pre-challenge sera to inhibit growth ofBorreliae, six representative strains expressing OspA types 1-6 (B31,Arcon, PBr, DK6, W, and KL11) were cultured at 33° C. in the presence ofserial dilutions of heat-inactivated peak titer serum pools ornon-immune mouse serum (negative control). B31 was cultured in thepresence of complement (guinea pig serum), while the other five strainswere tested in the absence of complement. Once again, growth inhibitionassays were carried out as described in Example 10. A standard serumpreparation was used to normalize titers between different assays.

Surface Binding and Growth Inhibiting Efficiency of Anti-OspA AntibodyResponses.

Intense fluorescence staining with MFI values, ranging from 50 to 200,was observed for all six Borrelia strains when tested with the threeserum pools derived from the different immunization dose groups (1.0,0.1 and 0.03 μg protein per dose) of the 3-component vaccine at adilution of 1:100 (FIG. 21). When the serum pools from the 3 dose groupswere tested for their capacity to inhibit bacterial growth, the3-component vaccine was also found to have induced strong GI-50 titersto all six OspA type strains, ranging from 1000 (type 4 strain, 0.03 μgdose) to 20,000 (type 6 strain).

Conclusion.

Taken together, these results demonstrate that the rOspA antigens arehighly immunogenic and induce large quantities of functional antibodieswhich can bind to the surface of live Borreliae and inhibit growth ofBorreliae. Coverage among the six strains tested was complete, as highfluorescence intensities and high growth inhibition titers weredetected, comparable to the levels observed for the OspA types 1 and 2.In summary, the results presented in this study indicate that antibodyresponses induced by the tri-component rOspA vaccine (1/2+5/3+6/4), whenformulated with Al(OH)3, prevent infections by strains expressing OspAtypes 1-6, which, as epidemiological studies have shown, theoreticallycovers over 99% of isolates causing human disease in Europe and NorthAmerica and, thus, is highly effective in preventing Lyme Borreliosis.

Example 14 A Vaccine Comprising the Three Component Vaccine (OspA 1/2,OspA 6/4, and OspA 5/3) is Required to Optimally Cover BorreliaExpressing OspA Types 1-6

The purpose of this study was to investigate and compare theimmunogenicity and the cross strain coverage of functional surfacebinding and/or growth inhibiting antibodies induced by single andmulti-component formulations of rOspA Lyme Borreliosis vaccine, againusing the efficiency of anti-OspA antibodies to bind to the surface oflive Borreliae and to inhibit growth of Borreliae in vitro as correlatesof protection

Immunization of Mice.

Ten female mice (C3H) per group were immunized with 0.1 μg of a singlecomponent vaccine comprising rOspA 1/2 antigen, rOspA 6/4 antigen, orrOspA 5/3 antigen; a two-component vaccine comprising 0.1 μg of both1/2+5/3 antigens, 1/2+6/4 antigens, or 5/3+6/4 antigens; or athree-component vaccine comprising a combination 0.1 μg of all three1/2+5/3+6/4 antigens adjuvanted with 0.2% Al(OH)3 in a prime-boosterregimen. Vaccination was carried out subcutaneously using a dose volumeof 200 μl on days 0, 14 and 28. On day 42, individual blood samples weretaken from mice to generate sera.

Antibody Surface Binding and Growth Inhibition Assays.

A slightly modified version of the surface binding assay was used todetermine the efficiency of anti-OspA IgG to bind to the surface of liveBorreliae. Serial dilutions of a serum pool with defined MFI titers wereincluded in the analyses to create a standard curve from which relativetiters of test sera were read off after interpolation with a non-linearregression curve. The MFI titer of standard serum for the individualstrains expressing OspA types 1-6 was defined as the highest dilution atwhich the fluorescence intensity of the Borreliae was determined to beat least 3-fold over the fluorescence intensity observed with normalmouse serum. All determinations were carried out in duplicate.

The scatter plots presented in FIG. 22 compare the MFI titers to the sixstrain expressing homologous OspA types observed for the immune sera ofindividual C3H mice after immunization with either single rOspA antigensor rOspA antigen combinations. Results showed that a formulationcontaining all three rOspA antigens (1/2, 5/3 and 6/4) was necessary toinduce high MFI titers against all six Borrelia strains expressing OspAtypes 1-6, and that formulations composed of two rOspA antigens (i.e.covering four strains) did not fully cover the strains expressing thetwo OspA types not present in the formulation.

To determine the potency of the various vaccine combinations to inducegrowth inhibiting antibodies, six representative Borreliae strains (B31,Arcon, PBr, DK6, W, KL11), expressing OspA types 1-6 respectively, werecultured at 33° C. in the presence of heat-inactivated immune ornon-immune mouse serum pools. All sera were tested at a single dilution.The following dilutions were used: B31, PBr and KL11 1:200, Arcon, DK6and W 1:100. PBr was cultured in the absence of 20% complement, whilethe other 5 strains were tested in the presence of complement. Babyrabbit complement was used for DK6, W and KL11, while guinea pig serumwas used for B31 and Arcon. When the bacteria in the control culturesincubated with non-immune sera had grown sufficiently, as determinedmicroscopically, accurate cell counts were made as described previously(see Example 10). The percentage of bacterial growth inhibition wascalculated from the cell count observed with test serum relative to thenormal mouse serum control. The overall growth inhibition observed forthe different formulations tested was then presented (FIG. 23) as thenumber of animals among the different groups of ten C3H mice that showedmore than 50% growth inhibition. Results demonstrated that the3-component formulation was the only formulation capable of inducinghigh titers of growth-inhibiting antibodies against all sixrepresentative strains expressing OspA types 1-6 (FIG. 23). In allcases, the 3-component vaccine formulation provided >50% growthinhibition in >90% of the immunized animals. The 2-component vaccineformulations did not fully cover the two strains expressing the OspAtypes not present in the vaccine. The formulation comprising rOspA1/2+6/4 did not cover the type 3 strain; the formulation comprisingrOspA 1/2+5/3 formulation did not cover types 4 or 6; and theformulation comprising rOspA 5/3+6/4 did not cover type 1.

Example 15 The Multivalent OspA Vaccine Formulation Covers BorreliaExpressing Intra-Type Variants or Subtypes of OspA Types 1-6

Although Borrelia OspA types 1-6 were selected as the basis for thedesign and construction of the multivalent rOspA vaccine, Borreliaewhich express OspA protein variants of types 1, 2, 3, 5, and 6 have alsobeen isolated. These variants, while being classified as being withinthe same type, have slightly altered nucleotide gene sequences and aminoacid protein sequences. Thus, intra-type variants or subtypes existamong OspA types 1, 2, 3, 5, and 6 (see FIG. 24). No intra-type variantor subtype has yet been observed for OspA type 4.

The purpose of this study was to confirm that immune serum generated byimmunizing mice with the 3-component multivalent rOspA vaccine containsfunctional antibodies which can bind to the surface of live Borreliaeexpressing these intra-type variants or subtypes.

For this study, a pooled mouse immune serum was generated by immunizing70 female C3H mice three times with 0.3 μg of the 3-componentmultivalent rOspA vaccine on days 0, 14 and 28. On day 42, mice werebled and serum was obtained and pooled. The pooled immune serum was thenused to test for binding of antibodies to the surface of live Borreliae.Borrelia cultures were incubated with the immune serum pool or controlnormal mouse serum at 1:100 in duplicate, and fluorescence intensitiesof Borreliae measuring binding of anti-OspA antibodies to the bacteriawas monitored by FACS analyses as described herein above.

High levels of surface binding antibodies (defined as a fluorescenceintensity of over 10 times that observed for a non-immunized mousecontrol serum) at a serum dilution of 1:100 were detected for most ofthe strains expressing OspA subtypes 1-6. In particular, high levels ofantibody binding were detected with Borreliae strains expressing OspAsub-types 1a, 1b, 1c, 1d, 1f, 1h, 1J, 1k, and 1l; 2a, 2b, 2e, 2g, 2k,2l, and 2n; 3a, 3c, 3d, and 3e; 5a and 5c; and 6a, 6e, 6f, 6g, and 6k(FIG. 24). Weaker binding (defined as a fluorescence intensity ofbetween 2-10 times that observed for a non-immunized mouse controlserum) was observed with Borreliae strains expressing OspA subtypes 1g,2j, 2m, 3b, 5d, and 6l (FIG. 24), but this weaker binding was primarilydue to the low expression of the OspA protein under the growthconditions used.

Conclusion.

The 3-component chimeric rOspA vaccine induces functional,surface-binding antibodies against all intra-type variants or subtypesof OspA types 1, 2, 3, 5, and 6 in C3H mice.

Example 16 The Multivalent OspA Vaccine Formulation Provides ProtectionAgainst Other Types of Borrelia in Addition to Those Expressing OspATypes 1-6

The purpose of this study was to determine if the 3-component chimericrOspA antigen vaccine formulation (comprising all 3 chimericantigens—1/2, 6/4, and 3/5) could also provide protection againstBorrelia expressing OspA types other than the homologous OspA types 1-6.40 C3H mice were immunized three times with 0.3 μg of the 3-componentvaccine on days 0, 14 and 28. On day 42, the mice were bled, and a serumpool was made and used to evaluate the efficiency of surface binding andgrowth inhibition against strains expressing heterologous OspA types.

The results of this study showed that the 3-component chimeric rOspAvaccine does induce antibodies which bind to the surface of Borreliaeand inhibit growth of other types of Borreliae, including strains of B.spielmanii, B. valaisiania, B. lusitaniae and B. japonica (see Table 9).In the case of B. garinii expressing OspA type 7, only weak surfacebinding and little or no growth inhibition was observed; however, thisweak binding and small amount of growth inhibition may be due to lowexpression levels of OspA under the in vitro culture conditions usedrather than to the lack of binding of immune serum antibodies.

TABLE 9 Surface Binding and Growth Inhibition against other types ofBorreliae B.g. B. B. B. B. Genotype OspA-7 spielmanii valaisianalusitaniae japonica Surface (+) + + + + Binding Growth − + + + +Inhibition +: significant surface binding and/or growth inhibition −: nosignificant binding/growth inhibition (+−): low intensity surfacebinding

Example 17 Multivalent OspA Vaccine Formulations Induces Antibodies to aCommon Epitope at the N-Terminus of the OspA Molecule which canContribute to Protection Against any OspA Expressing Borrelia Strain

During the course of investigating the protective efficacy ofmultivalent chimeric rOspA formulations, a monoclonal antibody(F237/BK2) was generated against a 2-component rOspA vaccine comprisingrOspA-1/2 and rOspA-6/4. F237/BK2 was shown by anti-OspA ELISA to bindto all OspA types investigated thus far (OspA types 1-7), as well as tothe 3 chimeric rOspA antigens (rOspA-1/2, rOspA-5/3 and rOspA-6/4) Suchresult indicate that F237/BK2 recognizes a common epitope found on allOspA molecules. Moreover, preliminary epitope mapping studies indicatethat this common epitope is located on the less variable N-terminal halfof the molecule (i.e. at the N-terminus of amino acid 130), where OspAsequence homologies are most commonly observed.

Interestingly, F237/BK2 was also shown to bind to the surface ofBorreliae expressing homologous OspA types 1-6 and heterologous OspAtypes, including those expressed by B. spielmanii, B. valaisiania and B.japonica, albeit less efficiently than monoclonal antibodies directedagainst C-terminal type-specific epitopes. Using methods similar tothose described in previous examples, F237/BK2 was also found to inhibitthe growth of representative strains expressing OspA types 1, 2, 4, 5and 6.

When F237/BK2 was tested in an in vivo passive protection model in mice,F237/BK2 was observed to confer protection against feral tick challenge,corresponding to a B. afzelii Type 2 challenge. Ticks were collected inWundschuh (Styria, Austria), which are known to be predominantlyinfected with B. afzelii. □ Ten female C3H mice were injectedintraperitoneally with 500 μg of affinity-purified mAb F237/BK2. Twohours later, 8 ticks were applied per animal to 10 passively immunizedmice as well as to 10 sham-immunized animals. Four days later, the fedticks were removed. On day 90, mice were sacrificed and analyzed forinfection by serological testing, PCR analysis and Borrelia culture, asdescribed herein above. No animal was infected in the group treated withF237/BK2, whereas 5 animals (50%) were infected with B. afzelii in thecontrol group. Thus, monoclonal antibody F237/BK2 provided statisticallysignificant (p=0.0325) passive protection against a tick challenge whencompared with the sham-immunized control mice. This is the first timethat a monoclonal antibody which binds to a common epitope on theN-terminal half of the molecule has been reported to be involved inprotection. Moreover, if a vaccine could induce antibodies recognizingthis common epitope, such an antibody would certainly contribute to thevaccine's cross protective efficacy.

To test whether such antibodies were indeed induced by the 3-componentchimeric rOspA vaccine formulation, a monoclonal antibody inhibitionELISA was carried out employing peroxidase-labeled F237/BK2. In theseexperiments, a GST-OspA type 3 protein was used as coating antigen, andeither normal mouse serum or a serum pool from C3H mice immunized threetimes with the 3-component chimeric rOspA vaccine was added to the wellsat a dilution of 1:100. Sixty minutes later, peroxidase-labeled F237/BK2was added at a pre-optimized concentration to eventually give an OpticalDensity (OD) value of around 1 for the non-inhibiting normal mouse serumcontrol, and incubation was continued for an additional 60 min. Finally,ELISA plates were washed and developed with TMB substrate.

Using this monoclonal antibody inhibition ELISA assay, it could bedemonstrated that the 3-component chimeric rOspA formulation does indeedinduce antibodies which bind to an epitope identical to or in closeproximity to the epitope recognized by mAb F237/BK2. OD values weresignificantly reduced (e.g., typically by 20-30%) by the anti-OspAimmune sera compared to the non-inhibiting normal mouse serum control.

Conclusion.

This study shows that the 3-component chimeric rOspA vaccine is able toinduce both a type-specific and a broad cross-protective immuneresponse.

Example 18 Additional Synthetic OspA Nucleic Acid and PolypeptideMolecules

The aim of the study was to design additional novel OspA antigenscomprising serotypes 1 and 2, 6 and 4, and 5 and 3, respectively. Threesynthetic OspA genes (SEQ ID NOS: 168 (orig sOspA 1/2), 170 (orig sOspA6/4), and 172 (orig sOspA 5/3)) were designed to encode OspA polypeptidemolecules with protective epitopes from OspA serotypes 1 and 2 (origsOspA 1/2), OspA serotypes 6 and 4 (orig sOspA 6/4) and OspA serotypes 5and 3 (orig sOspA 5/3) of Borrelia. The primary amino acid sequences ofthese molecules (SEQ ID NOS: 169, 171, and 173, respectively) areprovided in Table 1. These sequences comprise original chimericconstructs, i.e. without mutations and without codon optimization.

Example 19 Multivalent Recombinant OspA Formulation Comprising 3Antigens (1/2, 6/4, and 5/3) is Immunogenic in Mice

A multivalent OspA vaccine comprising original construct formulationswithout codon optimization and without mutations (orig OspA 1/2, origOspA 5/3, and orig OspA 6/4) is evaluated in a tick challenge model.Three recombinant OspA antigens containing the protective epitopes fromOspA serotypes 1 and 2 (SEQ ID NO: 169), OspA serotypes 6 and 4 (SEQ IDNO: 171), and OspA serotypes 5 and 3 (SEQ ID NO: 173) are combined in avaccine.

Groups of ten female C3H/HeJ mice (age at immunization: 11 weeks) areimmunized subcutaneously on days 0 and 28 with a fixed dose of 0.3 μg ofthe multivalent vaccine (0.1 μg of each, orig OspA 1/2, orig OspA 5/3,and orig OspA 6/4). The tick challenge is done as described herein abovewith ticks from Budweis, Czech Republic. The ability of the feral ticksto transmit B. burgdorferi s.l. to mice is confirmed by challengingun-immunized control animals. The infection status of the challengedmice is determined by Western blotting, real-time PCR, and by culture.

Interim blood samples are taken on day 41 by orbital puncture. Finalblood samples (day 70/71) are collected by heart puncture. Individualsera are prepared from whole blood by centrifugation (10 minutes;1000-2000×G; RT). Sera are stored at ≦−20° C. until use.

In this experiment unfed ticks, taken from the same batch used tochallenge the mice, are characterized to determine the overall infectionrate and to confirm the species of the infecting organisms.

Example 20 A Vaccine Comprising a Three-Component Vaccine (Orig OspA1/2, Orig OspA 6/4, and Orig OspA 5/3) Induces High Levels of FunctionalAnti-OspA Antibodies which Bind to and Inhibit Growth of BorreliaStrains Expressing OspA Types 1-6

The results presented in Example 13 indicate that antibody responsesinduced by the tri-component rOspA vaccine (lipB sOspA1/2+lipB sOspA5/3+lipB sOspA 6/4), when formulated with Al(OH)3, prevent infections bystrains expressing OspA types 1-6 and, therefore, are effective inpreventing Lyme Borreliosis. Thus, the present study is being carriedout to determine if equivalent functional immune responses are inducedby the tri-component OspA vaccine comprising chimeric original (orig)OspA antigens (Orig sOspA1/2+Orig sOspA 5/3+Orig sOspA 6/4).

Mouse Immunization.

Groups of 10 female C3H/HeJ mice are immunized subcutaneously threetimes (day 0, day 14, day 28) with a 1:1:1 mixture of Orig sOspA1/2+OrigsOspA 5/3+Orig sOspA 6/4) at three different doses (1, 0.1, 0.03 μgprotein per dose) combined with 0.2% Al(OH)3 as an adjuvant. Serum isgenerated from blood samples taken on day 40.

Quantitation of OspA Antibody Binding to the Surface of Live Borreliae.

In this assay, in vitro grown cultures of six representative Borreliastrains expressing OspA types 1-6 (B. burgdorferi sensu strictoB31/OspA-1; B. afzelii Arcon/OspA-2; B. garinii PBr/OspA-3; B. gariniiDK6/OspA-4; B. garinii W/OspA-5; and B. garinii KL11/OspA-6) areincubated at a fixed dilution (1:100) with pools of the peak titer mousesera at room temperature in the presence of EDTA to prevent complementactivation. The subsequent washing, labeling, detection and analysisprocedures are similar to those described in Examples 10 and 13. Normalmouse serum serves as a negative control for non-specific binding ofantibodies.

Bacterial Growth Inhibition Assay.

To measure the potency of the pre-challenge sera to inhibit growth ofBorreliae, six representative strains expressing OspA types 1-6 (B31,Arcon, PBr, DK6, W, and KL11) are cultured at 33° C. in the presence ofserial dilutions of heat-inactivated peak titer serum pools ornon-immune mouse serum (negative control). B31 is cultured in thepresence of complement (guinea pig serum), while the other five strainsare tested in the absence of complement. Growth inhibition assays arecarried out as described in Examples 10 and 13. A standard serumpreparation is used to normalize titers between different assays.

Surface Binding and Growth Inhibiting Efficiency of Anti-OspA AntibodyResponses.

Fluorescence staining is measured in all six Borrelia strains whentested with the three serum pools derived from the differentimmunization dose groups (1.0, 0.1 and 0.03 μg protein per dose) of the3-component vaccine at a dilution of 1:100.

Example 21 A Vaccine Comprising the Three Component Vaccine (OspA 1/2,OspA 6/4, and OspA 5/3) is Required to Optimally Cover BorreliaExpressing OspA Types 1-6

The purpose of this study is to investigate and compare theimmunogenicity and the cross strain coverage of functional surfacebinding and/or growth inhibiting antibodies induced by single andmulti-component formulations of Orig sOspA Lyme Borreliosis vaccineusing the efficiency of anti-OspA antibodies to bind to the surface oflive Borreliae and to inhibit growth of Borreliae in vitro as correlatesof protection

Immunization of Mice.

Ten female mice (C3H) per group are immunized with 0.1 μg of a singlecomponent vaccine comprising Orig sOspA1/2 antigen, Orig sOspA 5/3antigen, or Orig sOspA 6/4 antigen; a two-component vaccine comprising0.1 μg of both 1/2+5/3 antigens, 1/2+6/4 antigens, or 5/3+6/4 antigens;or a three-component vaccine comprising a combination 0.1 μg of allthree 1/2+5/3+6/4 antigens adjuvanted with 0.2% Al(OH)3 in aprime-booster regimen. Vaccination is carried out subcutaneously using adose volume of 200 μl on days 0, 14 and 28. On day 42, individual bloodsamples are taken from mice to generate sera.

Antibody Surface Binding and Growth Inhibition Assays.

A slightly modified version of the surface binding assay described aboveis used to determine the efficiency of anti-OspA IgG to bind to thesurface of live Borreliae. Serial dilutions of a serum pool with definedMFI titers are included in the analyses to create a standard curve fromwhich relative titers of test sera are read off after interpolation witha non-linear regression curve. The MFI titer of standard serum for theindividual strains expressing OspA types 1-6 is defined as the highestdilution at which the fluorescence intensity of the Borreliae isdetermined to be at least 3-fold over the fluorescence intensityobserved with normal mouse serum. All determinations are carried out induplicate.

To determine the potency of the various vaccine combinations to inducegrowth inhibiting antibodies, six representative Borreliae strains (B31,Arcon, PBr, DK6, W, KL11), expressing OspA types 1-6 respectively, arecultured at 33° C. in the presence of heat-inactivated immune ornon-immune mouse serum pools. All sera are tested at a single dilution.The following dilutions are used: B31, PBr and KL11 1:200, Arcon, DK6and W 1:100. PBr is cultured in the absence of 20% complement, while theother 5 strains are tested in the presence of complement. Baby rabbitcomplement is used for DK6, W and KL11, while guinea pig serum is usedfor B31 and Arcon. When the bacteria in the control cultures incubatedwith non-immune sera has grown sufficiently, as determinedmicroscopically, accurate cell counts are made as described previously(see Example 10). The percentage of bacterial growth inhibition iscalculated from the cell count observed with test serum relative to thenormal mouse serum control. The overall growth inhibition observed forthe different formulations tested is then presented as the number ofanimals among the different groups of ten C3H mice that showed more than50% growth inhibition.

Example 22 The Multivalent OspA Vaccine Formulation Covers BorreliaExpressing Intra-Type Variants or Subtypes of OspA Types 1-6

The purpose of this study was to confirm that immune serum generated byimmunizing mice with the 3-component multivalent orig OspA vaccine (origsOspA 1/2, orig sOspA 6/4, and orig sOspA 5/3) contains functionalantibodies which can bind to the surface of live Borreliae expressingthese intra-type variants or subtypes.

For this study, a pooled mouse immune serum is generated by immunizing70 female C3H mice three times with 0.3 μg of the 3-componentmultivalent orig OspA vaccine on days 0, 14 and 28. On day 42, mice arebled and serum is obtained and pooled. The pooled immune serum is thenused to test for binding of antibodies to the surface of live Borreliae.Borrelia cultures are incubated with the immune serum pool or controlnormal mouse serum at 1:100 in duplicate, and fluorescence intensitiesof Borreliae measuring binding of anti-OspA antibodies to the bacteriaare monitored by FACS analyses as described herein above.

The invention has been described in terms of particular embodimentsfound or proposed to comprise specific modes for the practice of theninvention. Various modifications and variations of the describedinvention will be apparent to those skilled in the art without departingfrom the scope and spirit of the invention. Although the invention hasbeen described in connection with specific embodiments, it should beunderstood that the invention as claimed should not be unduly limited tosuch specific embodiments. Indeed, various modifications of thedescribed modes for carrying out the invention that are obvious to thoseskilled in the relevant fields are intended to be within the scope ofthe following claims.

1-18. (canceled)
 19. An isolated polypeptide selected from the groupconsisting of: (a) an isolated polypeptide comprising an amino acidsequence having at least 90 percent sequence identity to the amino acidsequence set forth in SEQ ID NO: 2 or SEQ ID NO: 8; (b) an isolatedpolypeptide comprising the amino acid sequence set forth in SEQ ID NO:2or SEQ ID NO: 8; and (c) an isolated polypeptide consisting of the aminoacid sequence set forth in SEQ ID NO:2 or SEQ ID NO:
 8. 20-24.(canceled)
 25. A composition comprising the isolated polypeptide ofclaim 19 and a pharmaceutically acceptable carrier. 26-27. (canceled)28. An immunogenic composition comprising the composition of claim 25and a pharmaceutically acceptable carrier.
 29. The immunogeniccomposition of claim 28, wherein the composition induces production ofan antibody that specifically binds an outer surface protein (Osp) Aprotein.
 30. The immunogenic composition of claim 28, wherein thecomposition induces production of an antibody that specifically bindsBorrelia.
 31. The immunogenic composition of claim 28, wherein thecomposition induces production of an antibody that neutralizes Borrelia.32. The immunogenic composition of claim 30, wherein Borrelia isBorrelia burgdorferi sensu lato.
 33. The immunogenic composition ofclaim 30, wherein Borrelia is Borrelia afzelii, Borrelia garinii orBorrelia burgdorferi sensu stricto.
 34. The immunogenic composition ofclaim 30, wherein Borrelia is Borrelia japonica, Borrelia andersonii,Borrelia bissettii, Borrelia sinica, Borrelia turdi, Borrelia tanukii,Borrelia valaisiana, Borrelia lusitaniae, Borrelia spielmanii, Borreliamiyamotoi or Borrelia lonestar.
 35. A vaccine composition comprising theimmunogenic composition of claim 28 and a pharmaceutically acceptablecarrier. 36-40. (canceled)
 41. A method for inducing an immunologicalresponse in a subject, the method comprising the step of administeringthe composition of claim 28 to the subject in an amount effective toinduce an immunological response.
 42. The method of claim 41, whereinthe immunological response comprises production of an anti-OspAantibody.
 43. A method for preventing or treating a Borrelia infectionor Lyme disease in a subject, the method comprising the step ofadministering the vaccine composition of claim 35 to the subject in anamount effective to prevent or treat the Borrelia infection or Lymedisease. 44-51. (canceled)